Fish and seafood recalls: brands, lot codes and what to do
Short answer: FDA has listed 45 fish and seafood recalls reported since November 2024; the most recent was reported on Oct 28, 2026 (El Ruisenor De Mexico, Inc.). Recalls cover specific products, lots and dates. Compare your package with the list below.
Search all FDA food recalls by product, brand, UPC or lot code.
All 45 recalls
Recall details
El Ruisenor De Mexico, Inc. · Oct 28, 2026
- Product
- Dried Cod; packed in a clear plastic bag. 1lb, 5lb, 50lb unit size. No UPC
- Why it was recalled
- undeclared allergen ingredient (Fish) People who are allergic to fish or shellfish run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- lot: 440024553-11-001
- How many
- 102 pounds
- Where it was sold
- Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Aug 24, 2026; FDA classified it on Oct 20, 2026; reported in FDA's enforcement report on Oct 28, 2026.
- FDA recall number
- H-0111-2027
Shandong Ling Xian Food Co.,LTD · Jul 29, 2026
- Product
- Island Pacific IMITATION CRAB FLAKES NET WT: 1.0 LB (454g) UPC: 0000000175012 PRECOOKED SERVE HOT OR COLD INGREDIENTS: POLLOCK AND/OR THREADFIN BREAM, WATER, POTATO STARCH, TAPIOCA STARCH, CORN STARCH, SALT, SUGAR, MIRIN (RICE WINE), SOYBEAN OIL, SOYBEAN PROTEIN, CRAB EXTRACT, ARTIFICIAL CRAB FLAVOR, COLOR ADDED (CARMINE). CONTAINS: FISH (POLLACK AND/OR THREADFIN BREAM), CRUSTACEAN SHELLFISH (CRAB), AND SOYBEAN. PRODUCT OF CHINA ISLAND PACIFIC SUPERMARKET 738 Epperson Drive City of Industry CA 91748
- Why it was recalled
- Undeclared sodium tripolyphosphate (STTP)
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Crab Flake: 2603062605JS Expiration date for both products: 17/06/2026, 25/06/2026, 08/10/2027, 05/03/2028.
- How many
- 751 cartons
- Where it was sold
- Domestic Distribution: CA Foreign Distribution: Not Applicable
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jun 2, 2026; FDA classified it on Jul 21, 2026; reported in FDA's enforcement report on Jul 29, 2026.
- FDA recall number
- H-1184-2026
Shandong Ling Xian Food Co.,LTD · Jul 29, 2026
- Product
- Island Pacific IMITATION CRAB STICKS NET WT: 1.0 LB (454g) UPC: 0000000175029 PRECOOKED SERVE HOT OR COLD INGREDIENTS: POLLOCK AND/OR THREADFIN BREAM, WATER, POTATO STARCH, TAPIOCA STARCH, CORN STARCH, SALT, SUGAR, MIRIN (RICE WINE), SOYBEAN OIL, SOYBEAN PROTEIN, CRAB EXTRACT, ARTIFICIAL CRAB FLAVOR, COLOR ADDED (CARMINE). CONTAINS: FISH (POLLACK AND/OR THREADFIN BREAM), CRUSTACEAN SHELLFISH (CRAB), AND SOYBEAN. PRODUCT OF CHINA ISLAND PACIFIC SUPERMARKET 738 Epperson Drive City of Industry CA 91748
- Why it was recalled
- Undeclared sodium tripolyphosphate (STTP)
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Crab Stick Lot No.: 2412292402HS
- How many
- 751 cartons
- Where it was sold
- Domestic Distribution: CA Foreign Distribution: Not Applicable
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jun 2, 2026; FDA classified it on Jul 21, 2026; reported in FDA's enforcement report on Jul 29, 2026.
- FDA recall number
- H-1182-2026
Shandong Ling Xian Food Co.,LTD · Jul 29, 2026
- Product
- NAUTILUS IMITATION CRAB STICKS NET WT: 1.0 LB (454.0g) UPC: 878665000235 Precooked - serve hot or cold Ingredients: Pollock and/or threadfin bream, water, potato starch, tapioca starch, corn starch, wheat starch, eggs, salt, sugar, mirin (rice wine), soybean oil, soybean protein, crab extract, artificial crab flavor, cochineal color (E-120), paprika color (E-160C). Contains: Fish (Pollock and/or threadfin bream), egg, crustacean shellfish (crab), wheat and soybean. Product of China Packed For: NAUTILUS SEAFOODS WILMINGTON, CA 90744
- Why it was recalled
- Undeclared sodium tripolyphosphate (STTP)
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Crab Stick: 2406182402HS, 2406262402HS, 2510092507HS, 2603062605JS.
- How many
- 4477 cartons
- Where it was sold
- Domestic Distribution: CA Foreign Distribution: Not Applicable
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jun 2, 2026; FDA classified it on Jul 21, 2026; reported in FDA's enforcement report on Jul 29, 2026.
- FDA recall number
- H-1183-2026
Prime Food Processing LLC. · Jul 1, 2026
- Product
- Dried Herring Fish 7 oz.
- Why it was recalled
- Improperly eviscerated which may result in Clostridium botulinum contamination Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Lot Code: 26020. Expiration: 06.12.28 UPC Codes: 6946976817911
- How many
- 69 cases
- Where it was sold
- AZ, CA, FL, HI, IL, KS, LA, MD, MO, NC, NH, NV, NY, OK, OR, PA, TX, UT, WA
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jun 2, 2026; FDA classified it on Jun 22, 2026; reported in FDA's enforcement report on Jul 1, 2026.
- FDA recall number
- H-1080-2026
Boichik Bagels, Inc. · Jul 1, 2026
- Product
- boichik bagels Whitefish Salad Ingredients: Smoked whitefish, mayonnaise (soybean oil, water, whole eggs and egg yolks, distilled vinegar, salt, sugar, lemon juice concentrate, calcium disodium edta, natural flavors), pickle juice, mustard, chives, black pepper. Contains: Fish
- Why it was recalled
- Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Sell By: 05-22-26, 05-23-26, 05-24-26, 05-25-26, 05-27-26, 05-28-26, 05-29-26, 05-30-26, 05-31-26, 06-01-26, 06-02-26, 06-03-26, 06-04-26
- How many
- 167 containers
- Where it was sold
- Domestic: CA Foreign: Not applicable
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started May 22, 2026; FDA classified it on Jul 1, 2026; reported in FDA's enforcement report on Jul 1, 2026.
- FDA recall number
- H-1131-2026
Boichik Bagels, Inc. · Jul 1, 2026
- Product
- boichik bagles Tuna Salad Ingredients: albacore tuna, mayonnaise (soybean oil, water, whole eggs and egg yolks, distilled vinegar, salt, sugar, lemon juice concentrate, calcium disodium edta, natural flavors), pickle juice, mustard, chives, black pepper. Contains: Fish
- Why it was recalled
- Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Sell By: 05-22-26, 05-23-26, 05-24-26, 05-25-26, 05-27-26, 05-28-26, 05-29-26, 05-30-26, 05-31-26, 06-01-26, 06-02-26, 06-03-26, 06-04-26
- How many
- 164 containers
- Where it was sold
- Domestic: CA Foreign: Not applicable
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started May 22, 2026; FDA classified it on Jul 1, 2026; reported in FDA's enforcement report on Jul 1, 2026.
- FDA recall number
- H-1132-2026
Albertsons Companies LLC · Jun 10, 2026
- Product
- UPC 21234900000 TILAPIA PARMESAN CRUSTED SS COLD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
- Why it was recalled
- Contains statement does not declare Tilapia
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Product was labeled with a Packed On date of May 05. 26 or before.
- How many
- 15 units
- Where it was sold
- Nationwide.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started May 6, 2026; FDA classified it on Jun 18, 2026; reported in FDA's enforcement report on Jun 10, 2026.
- FDA recall number
- H-1039-2026
Albertsons Companies LLC · Jun 10, 2026
- Product
- UPC 27183100000 Ready Meals DUO SEAFOOD SALAD W/CRACKERS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
- Why it was recalled
- Contains statement does not declare Whiting
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Product was labeled with a Packed On date of May 05. 26 or before.
- How many
- 286 units
- Where it was sold
- Nationwide.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started May 6, 2026; FDA classified it on Jun 18, 2026; reported in FDA's enforcement report on Jun 10, 2026.
- FDA recall number
- H-1012-2026
Terra Medi LLC · Jun 10, 2026
- Product
- Hellas Meze Golden Smoked Whole Herring
- Why it was recalled
- Un-eviscerated fish may be contaminated with clostridium botulinum Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- production date of 4/12/2025, best before 4/12/2026, L120425F54
- How many
- 20 cases (15 units per case)
- Where it was sold
- MA, NJ, IL, and NY
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started May 13, 2026; FDA classified it on Jun 2, 2026; reported in FDA's enforcement report on Jun 10, 2026.
- FDA recall number
- H-0899-2026
Albertsons Companies LLC · Jun 10, 2026
- Product
- UPC 29477800000 Ready Meals SALAD SEAFOOD CAJUN SS COLD UPC 29477600000 SALAD SEAFOOD CAJUN FS COLD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
- Why it was recalled
- Contains statement does not declare Crab and Pollock
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Product was labeled with a Packed On date of May 05. 26 or before.
- How many
- 110 units
- Where it was sold
- Nationwide.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started May 6, 2026; FDA classified it on Jun 18, 2026; reported in FDA's enforcement report on Jun 10, 2026.
- FDA recall number
- H-1014-2026
Albertsons Companies LLC · Jun 10, 2026
- Product
- UPC 23625000000 FISH HOUSE PREMIUM SEAFOOD SALAD UPC 21431200000 Ready Meals SALAD SEAFOOD SS UPC 21878600000 SALAD SEAFOOD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
- Why it was recalled
- Contains statement does not declare Crab
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Product was labeled with a Packed On date of May 05. 26 or before.
- How many
- 114 units total
- Where it was sold
- Nationwide.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started May 6, 2026; FDA classified it on Jun 18, 2026; reported in FDA's enforcement report on Jun 10, 2026.
- FDA recall number
- H-1013-2026
Albertsons Companies LLC · Jun 10, 2026
- Product
- UPC 23308200000 TILAPIA TORTILLA CRUSTED This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
- Why it was recalled
- Contains statement does not declare Tilapia
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Product was labeled with a Packed On date of May 05. 26 or before.
- How many
- 208 units
- Where it was sold
- Nationwide.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started May 6, 2026; FDA classified it on Jun 18, 2026; reported in FDA's enforcement report on Jun 10, 2026.
- FDA recall number
- H-1040-2026
Albertsons Companies LLC · Jun 10, 2026
- Product
- UPC 23114800000 SEAFOOD SALAD IMITATION CAJUN CRAB This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
- Why it was recalled
- Contains statement does not declare Crab and Pollock
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Product was labeled with a Packed On date of May 05. 26 or before.
- How many
- 53 units
- Where it was sold
- Nationwide.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started May 6, 2026; FDA classified it on Jun 18, 2026; reported in FDA's enforcement report on Jun 10, 2026.
- FDA recall number
- H-1015-2026
Shining Sea Fish Co. LLC · May 27, 2026
- Product
- MA Cohen's Kippered Herring vacuum packed, weight provided at retail, UPC 7232577992
- Why it was recalled
- Clostridium botulinum is an uncontrolled hazard Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- LOT 25079 Expiration May 03 2026, LOT 25055 Expiration May 12 2026, LOT 25028 Expiration June 03 2026, LOT 26344 Expiration July 22 2026
- How many
- 675 pounds
- Where it was sold
- MI
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 28, 2026; FDA classified it on May 20, 2026; reported in FDA's enforcement report on May 27, 2026.
- FDA recall number
- H-0810-2026
Booey's Gourmet LLC · Apr 22, 2026
- Product
- Booey's Dragon's Breath sauce, 15.2oz ringneck glass bottle. UPC on bottle: 7 01936 29222 3. There are 12 bottles per case. Manufactured Exclusively for BOOEYS GOURMET 3924 N. Cannon St. Spokane, WA 99205. Label declares: INGREDIENTS: Contains Soy and Wheat. *** Soy Sauce (Water, Soybeans, Wheat, Salt ***Squid Sauce (Anchovy Extract) ***Sesame Oil***.
- Why it was recalled
- Ingredients statement declares Anchovy and Sasame, but Contains statement does not declare Fish (Anchovy) and Sesame.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- None
- How many
- 870 bottles
- Where it was sold
- Distributed in WA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Mar 23, 2026; FDA classified it on Apr 15, 2026; reported in FDA's enforcement report on Apr 22, 2026.
- FDA recall number
- H-0665-2026
Riverence Provisions LLC · Apr 15, 2026
- Product
- Riverence Smoked Trout Dip, net wt. 7oz. Product is perishable, refrigerated, packaged in plastic tub. Product is shipped to consignee frozen by the case (12/7oz. units per case). Retail container UPC 7 07651 30561 3. Case item UPC #007076513057 Label declares Ingredients: Smoked Trout, Whipped Cream Cheese, Sour Cream, Horseradish, Lemon Juice, Dill, Black Pepper. Contains: Fish (Rainbow Trout).
- Why it was recalled
- Label declares cream cheese but does not declare milk
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot #25339, 26037, and 26057. Best By Dates: 12/5/2026, 8/6/2027, and 8/27/2027 is marked on the side of the case. However, these best before dates are for the cases while the product is frozen. Once an individual unit is moved out of the case and into refrigeration the shelf life is 45-days. Therefore, the consumer of an individual unit will not see the best before dates associated with a case of frozen product. Direct consignees were instructed to add a best before date to an individual unit based on the date moved from a freezer to a refrigerator.
- How many
- 306 cases (3,672 units)
- Where it was sold
- Distributed in CA, MA, NJ, NY, OR, TX, UT, VT.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Mar 19, 2026; FDA classified it on Apr 14, 2026; reported in FDA's enforcement report on Apr 15, 2026.
- FDA recall number
- H-0662-2026
MIN JIANG FOOD STORE INC DBA KOI KOI TRADING · Mar 4, 2026
- Product
- Fish Ball, Frozen, 40 pieces per pack, 200g Wt. UPC# 810093891338
- Why it was recalled
- Undeclared allergen ingredient (Wheat and Sesame) People who are allergic to wheat, or who have celiac disease, run the risk of a serious reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Item# 27010
- How many
- 344 cases
- Where it was sold
- Product was distributed to 50 consignees across the following states; CA, HI, TX, CO, GA, OR, NJ, WA. Product was primarily distributed to restaurants and retail grocery stores.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 28, 2026; FDA classified it on Feb 26, 2026; reported in FDA's enforcement report on Mar 4, 2026.
- FDA recall number
- H-0530-2026
MIN JIANG FOOD STORE INC DBA KOI KOI TRADING · Mar 4, 2026
- Product
- Fish Ball, Frozen, 4 pieces per pack, 5lbs Wt. UPC# 810093891320
- Why it was recalled
- Undeclared allergen ingredient (Wheat and Sesame) People who are allergic to wheat, or who have celiac disease, run the risk of a serious reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Item# 27530 Expiration: 11/11/2027
- How many
- 8,232 case
- Where it was sold
- Product was distributed to 50 consignees across the following states; CA, HI, TX, CO, GA, OR, NJ, WA. Product was primarily distributed to restaurants and retail grocery stores.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 28, 2026; FDA classified it on Feb 26, 2026; reported in FDA's enforcement report on Mar 4, 2026.
- FDA recall number
- H-0532-2026
MIN JIANG FOOD STORE INC DBA KOI KOI TRADING · Mar 4, 2026
- Product
- Fish Ball, Frozen, 20 pieces per pack, 400g Wt. UPC# 810093891325
- Why it was recalled
- Undeclared allergen ingredient (Wheat and Sesame) People who are allergic to wheat, or who have celiac disease, run the risk of a serious reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Item# 27550
- How many
- 3,884 cases
- Where it was sold
- Product was distributed to 50 consignees across the following states; CA, HI, TX, CO, GA, OR, NJ, WA. Product was primarily distributed to restaurants and retail grocery stores.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 28, 2026; FDA classified it on Feb 26, 2026; reported in FDA's enforcement report on Mar 4, 2026.
- FDA recall number
- H-0531-2026
Prime Food Processing LLC. · Mar 4, 2026
- Product
- Prime Food Processing Dried Croaker Fish; NET WT: 8oz (227g); Ingredients: Croaker Fish, Salt; CONTAINS: FISH (CROAKER FISH); DISTRIBUTED BY: PFP LLC, Brooklyn, NY, 11211, USA; Product must be thoroughly cleaned and cooked before consumption.; PRODUCT OF VIETNAM; UPC: 6 946976 818000
- Why it was recalled
- Uneviscerated Fish
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Item #AF1410 Expiration: 12-28-27 UPC Codes: #946976818000
- How many
- 79 cases
- Where it was sold
- AZ, CA, FL, GA, HI, ID, MA, MD, MO, NJ, NV, NY, OH, OK, PA, VA, WA, WI
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Feb 3, 2026; FDA classified it on Feb 20, 2026; reported in FDA's enforcement report on Mar 4, 2026.
- FDA recall number
- H-0519-2026
Reser's Fine Foods, Inc. · Feb 25, 2026
- Product
- The Tuna Salad product container is mislabeled with a Chicken Salad lid, which states: Molly Kitchen's Chicken Salad, 789953, NET WT. 5 LB (2.26 kg) per plastic tub. UPC 7 5810830149 8. Distributed by US Foods, Inc. Rosemont, IL 60018. The lid declares Contains: Eggs, Milk, Wheat. The immediate 5-lb tub has no side labeling (besides the lid). The master cardboard case label is correct and states: Molly Kitchen's Tuna Salad, (item #) 794599, 2/5 LB tubs per case, Net Wt. 10 LB (4.53 kg). UPC 075810876447. Distributed by US Foods, Inc. Rosemont, IL 60018. Contains: Egg, Wheat, Fish (Tuna).
- Why it was recalled
- Undeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad. People who are allergic to fish or shellfish run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Lot 1410100754 Use By FEB/21/26
- How many
- 149 cases (2 tubs /case) or 298 total tubs
- Where it was sold
- Distributed in AZ, CA, NV, UT and WA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 30, 2026; FDA classified it on Feb 19, 2026; reported in FDA's enforcement report on Feb 25, 2026.
- FDA recall number
- H-0517-2026
GOLD STAR DISTRIBUTION INC · Jan 28, 2026
- Product
- All human food products distributed from the firm. Including but not limited to: snack foods, candy, gum, cooking oil, canned fruit and beans, honey, Dietary supplements, peanut butter, oatmeal, rice, dry peas and beans, ramen, cold cereal, hot sauce, lemon juice, crackers, canned sardines tuna and Oyster, sauces, seasonings, sugar, bottled and canned beverages, coffee and filters and creamer, tea bags, canned pasta, dates, flour, baby food
- Why it was recalled
- Potential exposure of rodents and rodent activity in the distribution center.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- all codes of products purchased from this firm.
- How many
- unknown
- Where it was sold
- IN, MN, ND
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Dec 26, 2025; FDA classified it on Jan 22, 2026; reported in FDA's enforcement report on Jan 28, 2026.
- FDA recall number
- H-0411-2026
Kosher First LLC · Dec 17, 2025
- Product
- Shloimy's Heimishe Matjes Herring packaged in 7oz plastic container
- Why it was recalled
- Undeclared FD&C Red #40
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Batch Code: 0103
- How many
- 283 units
- Where it was sold
- New York
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Nov 10, 2025; FDA classified it on Dec 5, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0238-2026
African Food on Wheels Inc. · Dec 17, 2025
- Product
- Oven Dried Fish (SCOMBEROMORUS CAVALLA); distributed to walk-in customers of African Food on Wheels Inc. located at 1376 Randall Avenue, Bronx, NY 10474 only; Product is packed in a corrugated brown box.
- Why it was recalled
- Clostridium botulinum (uneviscerated fish) Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- No codes
- How many
- 20 Boxes
- Where it was sold
- Distributed to walk-in customers of African Food on Wheels Inc. located at 1376 Randall Avenue, Bronx, NY 10474 only
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Nov 5, 2025; FDA classified it on Dec 5, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0237-2026
Pacific Seafood - Portland, LLC · Dec 10, 2025
- Product
- Pacific Seafood Raw Blackened Shrimp Peeled & Deveined Tail-Off, refrigerated, farm-raised. Net wt. per tray 8 oz (227 g). UPC 0 27241 44630 5. Ingredients: Shrimp (Shrimp, Water, Salt, Sodium tripolyphosphate (to retain moisture), Blackened Seasoning (Sea Salt, Paprika, Spices, Onion, Garlic, Paprika Extract). CONTAINS: Shrimp (Crustacean Shellfish). Product of Ecuador. Packed and distributed by Pacific Seafood Group Clackamas, OR.
- Why it was recalled
- Undeclared Sulfite. Shrimp may contain 3.4mg Sulfur Dioxide per serving and label does not declare Sulfite.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot Numbers: 4211281; 4210119; 4209823
- How many
- Total of 15,498 lbs.
- Where it was sold
- Distributed in AL, FL, and MA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 8, 2025; FDA classified it on Dec 3, 2025; reported in FDA's enforcement report on Dec 10, 2025.
- FDA recall number
- H-0226-2026
New Hoque and Sons, Inc. · Nov 26, 2025
- Product
- Dry Ghoinnya Fish
- Why it was recalled
- Un-eviscerated fish may be contaminated with Clostridia botulinum. Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Expiration date of 5/19/25 UPC code is 908172635412.
- How many
- 5 cases (10 - 12 lbs. per case)
- Where it was sold
- NY, NJ
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Oct 28, 2025; FDA classified it on Nov 19, 2025; reported in FDA's enforcement report on Nov 26, 2025.
- FDA recall number
- H-0202-2026
Ocean's Kitchen Corp. · Oct 29, 2025
- Product
- Oceans Kitchen IMITATION CRABMEAT SHREDDED Made From Wild Fish, Refrigerated, vacuum package. Net wt. per bag 2.5 lbs. UPC 1 90456 75654 2. These 2.5lb. bags are not for retail sales. Each master case contains 12/2.5lbs. bags. Net wt. per case: 30lbs. UPC 14972195756549. Oceans Kitchen Corporation, 7622 S 188TH ST., KENT, WA 98032
- Why it was recalled
- The potential contamination with Clostridium botulinum, due to risk of temperature abuse during chilled storage at the firm. Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- USE BY OCT 23 2025 Best If Used By: 10/23/2025 Lot #CH062525 USE BY OCT 31 2025 Best If Used By: 10/31/2025 Lot # CH070325 USE BY NOV 6 2025 Best If Used By: 11/6/2025 Lot # CH070925
- How many
- 496 cases (12/2.5lb. bags per case)
- Where it was sold
- Distributed in WA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Sep 30, 2025; FDA classified it on Oct 27, 2025; reported in FDA's enforcement report on Oct 29, 2025.
- FDA recall number
- H-0140-2026
ONE FROZEN, LLC · Oct 22, 2025
- Product
- Good and Gather brand Southwest-Style Burrito Bowl Blend Processed in a facility that also handles shellfish, egg, fish, milk, sesame, soy, tree nut and wheat ingredients
- Why it was recalled
- Product may contain undeclared shrimp (crustacean shellfish). People who are allergic to fish or shellfish run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: 5505-1 and 5505-2
- How many
- 57,240 bags
- Where it was sold
- Nationwide.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Sep 4, 2025; FDA classified it on Oct 10, 2025; reported in FDA's enforcement report on Oct 22, 2025.
- FDA recall number
- H-0042-2026
Vicky IT Inc. · Oct 22, 2025
- Product
- Bona Fish
- Why it was recalled
- Fish is un-eviscerated (may be contaminated with Clostridia botulinum), is contaminated with mold, and contains filth (insect larvae) Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- no codes
- How many
- 10 lbs.
- Where it was sold
- NY
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Sep 27, 2025; FDA classified it on Oct 24, 2025; reported in FDA's enforcement report on Oct 22, 2025.
- FDA recall number
- H-0133-2026
Lee K of NY Inc. · Oct 15, 2025
- Product
- PINOCCHIO CATERING Aged Kimchi Mackerel; 57oz; 27330700000 in black bottomed plastic container
- Why it was recalled
- Product contains undeclared milk and shrimp People who are allergic or sensitive to milk run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Expiration dates prior to 09/16/25.
- How many
- 43 units
- Where it was sold
- NY and NJ
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Sep 8, 2025; FDA classified it on Oct 7, 2025; reported in FDA's enforcement report on Oct 15, 2025.
- FDA recall number
- H-0024-2026
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- HI-TECH PHARMACEUTICALS FISH OIL HEART AND BRAIN HEALTH EPA/DHA OMEGA 3 FATTY ACIDS SUPPORTS CARDIOVASCULAR HEALTH MAY HELP WITH JOINT PAIN MAY IMPROVE COGNITIVE FUNCTION 90 SOFT GELS UPC 8 11836 02585 9 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
- Why it was recalled
- Unapproved Drug Claims.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot 517120551 Exp Date 04/30
- How many
- 85,950 units total
- Where it was sold
- Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0589-2025
TAMPA MAID FOODS, LLC · Sep 10, 2025
- Product
- ADMIRAL OF THE FLEET and PORTICO SEAFOOD CLASSIC (SYSCO) Cleantail Breaded Butterfly Shrimp (16/20 CT per pound) in bulk packaging, corrugated master cartons. Master carton case is NET WT 12 lbs. (192 OZ) 5.44 kg (4 x 3lbs cartons), and carton case (4 x 3lb (1.36 kg), KEEP FROZEN. Farm Raised Clean Tail. Product of Indonesia. Item# 1SH01502017 and 1SH0452209H and 1SH05304085
- Why it was recalled
- Product may be contaminated with Cesium-137 (Cs-137)
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Corresponding Customer Lot Codes (visible on cases) 505611R and 505811R and 01245 BMS / 01345 BMS / 01445 BMS
- How many
- 1200 cases
- Where it was sold
- Product was distributed to OH, MI, WI, PA, TX, MN, SC, OK, TN, MI, IL, KY, FL, VA,
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 16, 2025; FDA classified it on Sep 2, 2025; reported in FDA's enforcement report on Sep 10, 2025.
- FDA recall number
- H-0552-2025
Krasnyi Oktyabr USA Inc · Aug 13, 2025
- Product
- ARAL FISH; ARAL SILVER VOBLA; WHOLE DRIED, SALTED ROACH FISH EVISCERATED; FISH ROE DRIED; Ingredients: whole eviscerated dried roach fish, caviar may be present, salt.; Distributed by Krasnyi Oktyabr; PERISHABLE KEEP REFRIGERATED AT OR BELOW 40F; PRODUCT OF KAZAKHSTAN
- Why it was recalled
- Clostridium botulinum (uneviscerated fish) Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- No Codes
- How many
- 23 boxes
- Where it was sold
- AZ, CA, CO, FL, GA, KS, MA, MI, MN, MO, NY, OH, PA, TX, WA, WI
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jun 18, 2025; FDA classified it on Aug 6, 2025; reported in FDA's enforcement report on Aug 13, 2025.
- FDA recall number
- H-0391-2025
P East Trading Corp · Jul 2, 2025
- Product
- Salted Smoked Split Herring, approximately 12 inches in length; packaged in 18 lb wooden box and repacked at retail in deli-style or other retail packaging (for a list of retail locations see associated press release)
- Why it was recalled
- Clostridium botulinum (uneviscerated fish) Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Lot: 1PRC5073
- How many
- 81 cases
- Where it was sold
- NY, NJ, CT
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jun 6, 2025; FDA classified it on Jun 24, 2025; reported in FDA's enforcement report on Jul 2, 2025.
- FDA recall number
- H-0067-2025
Homegrown Family Foods LLC · Jul 2, 2025
- Product
- Shore Lunch BREADING & BATTER MIX OVEN STYLE A savory, crunchy coating perfect for fish, pork and chicken. Net Wt 6oz (170g) UPC 0 24739 12000 6 Summit Hill Foods Rome, GA 30162
- Why it was recalled
- Undeclared Milk. People who are allergic or sensitive to milk run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- LOT# RP117050, LOT# RP120012, LOT# RP120011, LOT# RP120013, LOT# RP123249, LOT# RP123389, LOT# RP129004, LOT# RP129005, LOT# RP129006
- How many
- 7811 cs/10 cartons per cs
- Where it was sold
- Product was shipped to the following states: IA, IL, IN, MN, ND, NE, NY, OH, SD, WI
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started May 9, 2025; FDA classified it on Jun 20, 2025; reported in FDA's enforcement report on Jul 2, 2025.
- FDA recall number
- H-0063-2025
Bornstein Seafoods Inc · Jul 2, 2025
- Product
- Bornstein Frozen Shrimp Meat, Wild Caught - Product of USA. Product is cooked and Ready-To-Eat. Processed in the USA by Bornstein Seafoods Inc. Astoria, OR. The following items are being recalled: ZMU41-1003 Fzn Shrimp Meat 250/350 Ct 15 X 1lb. bag (net wt. 15lb) ZMU41-1007 Fzn Shrimp Meat 250/350 Ct 4 X 5lb. bag (net wt. 20lb) ZMU41-1015 Fzn Shrimp Meat 350/500 Ct 15 X 1lb. bag (net wt. 15lb) ZMU41-1019 Fzn Shrimp Meat 350/500 Ct 4 X 5lb bag (net wt. 20lb) ZMU41-1020 Fzn Shrimp Meat 350/500 Ct 20lb bag (net wt. 20lb) ZMU41-1045 Fzn Shrimp Meat 250/350 Ct 20lb bag (net wt. 20lb)
- Why it was recalled
- The recall was the result of the firm's routine sampling program and Listeria monocytogenes was detected in an in-process shrimp sample in a food production environment. Listeria monocytogenes can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy people may have short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. Listeria infection can cause miscarriages and stillbirths.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Item ZMU41-1003: Lot A19008 Item ZMU41-1007: Lot A18984, A19002, A19006, A19007, A19008, A19009, P11709, P11710, and P11714. Item ZMU41-1015: Lot A19009, A19019, A19026, A19030, A19032, A19037, and A19039. Item ZMU41-1019: Lot A18989, A19006, A19007, P11709, and P11710. Item ZMU41-1020: A19060 A19061 A19063 A19065 A19070 A19075 A19077 A19081 A19082 A19084 A19093 A19094 A19095 A19108 A19119 P11720 P11722 P11723 P11724 Item ZMU41-1045: A19030 A19032 A19033 A19037 A19039 A19060 A19063 A19064 A19065 A19068 A19069 A19070 A19075 A19076 A19082 A19084 A19094 A19108 P11709¿¿¿¿¿¿ P11722 P11724 P11730 Pl1723
- How many
- Total 452,875 lbs.
- Where it was sold
- Distributed nationwide and in Canada.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jun 4, 2025; FDA classified it on Jun 25, 2025; reported in FDA's enforcement report on Jul 2, 2025.
- FDA recall number
- H-0069-2025
Vern's Foods & Farm · Jun 18, 2025
- Product
- Taylor Shellfish Farms Geoduck Chowder Base, frozen, Ingredients: Potatoes, Clam (Geoduck) ***Butter (Cream, Salt), Fish Sauce Ka Me***CONTAINS: MILK, CLAMS. Product is packed in rigid plastic tubs. Net wt. 16 oz. Produced with local, farm fresh ingredients by: Vern's Foods & Farm, 4419 Harrison Ave. NW #104, Olympia WA 98502
- Why it was recalled
- The ingredients statement declares fish sauce but does not declare anchovies. The Contains statement does not declare fish (anchovies).
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Use By 7-19-25
- How many
- 48/16oz. cans
- Where it was sold
- Distributed in WA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started May 7, 2025; FDA classified it on Jun 11, 2025; reported in FDA's enforcement report on Jun 18, 2025.
- FDA recall number
- F-0937-2025
Santa Monica Seafood Company · Jun 18, 2025
- Product
- Atlantic Salmon Portions with Seafood Stuffing; 16 OZ (1 LB) 454g; Use/Freeze By: JUN.02.25; UPC: 4061459716313
- Why it was recalled
- Atlantic Salmon Portions with Seafood Stuffing was incorrectly labeled and does not declare allergen ingredient (SOY)
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Lot#: 197940521
- How many
- 150 cases
- Where it was sold
- Product is a private label exclusively for Aldi Inc. Firm is still collecting distribution information and number of retail locations that received product.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started May 24, 2025; FDA classified it on Jun 12, 2025; reported in FDA's enforcement report on Jun 18, 2025.
- FDA recall number
- H-0043-2025
Caraluzzi's Markets · May 7, 2025
- Product
- Caraluzzi's Italian Style Seafood Burgers, 8oz; INGREDIENTS: Cod, Salmon, Shrimp, Scallops, Onions, Olive Oil, White Wine, Parsley, Sodium Caseinate (A Milk Derivative), Spices, Garlic, Salt, Paprika, Enzyme.; CONTAINS: Crustacean Shellfish, Fish, Milk; Distributed by Caraluzzi's Markets, Bethel, CT 06801; UPC: 0 95864 80008 8
- Why it was recalled
- Product contains undeclared egg. People who are allergic to eggs run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Expiration: 1/16/2026
- How many
- 79 units
- Where it was sold
- CT
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 2, 2025; FDA classified it on Apr 30, 2025; reported in FDA's enforcement report on May 7, 2025.
- FDA recall number
- F-0747-2025
Chicken of the Sea; Thai Union · Mar 19, 2025
- Product
- Genova branded Solid white Tuna; In Olive Oil; Wild Caught; NET WT. 5 OZ (142g) RD WT. 4 OZ (113g); Distributed by Tri-Union Seafoods, LLC.; El Sugundo, CA 90245 U.S.A. UPC# 48000 00215,
- Why it was recalled
- Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum. Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Best By dates: 12/12/2027, 01/24/2028 Lots: S94N 42K; S94N 43K; S94N 44K; S94N D1L flat of 24- 5 ounce individual cans: 01/13/2028 ;01/17/2028; 01/24/2028; 12/12/2027; 01/21/2028; 01/27/2028 Lots: S84ND1N; S84ND2M; S84ND4H; S88ND1M; S94N42K; S94N43K; S94N44K; S94ND1M; S94ND1L Shrink wrapped 6- 7 ounce can pack: 01/21/2028; 01/23/2028; 01/27/2028 Lots: S84ND1D; S84ND3D; S84ND2D
- How many
- 14,147 cases total
- Where it was sold
- Product was distributed nationwide.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Feb 4, 2025; FDA classified it on Mar 11, 2025; reported in FDA's enforcement report on Mar 19, 2025.
- FDA recall number
- F-0610-2025
Chicken of the Sea; Thai Union · Mar 19, 2025
- Product
- Genova branded Yellowfin Tuna; Genova; In Olive Oil; Wild Caught; NET WT. 5 OZ (142g) RD WT. 4 OZ (113g); Distributed by Tri-Union Seafoods, LLC.; El Sugundo, CA 90245 U.S.A. UPC# 48000 73265 UPC# 48000 13265 UPC# 48000 63267 Product is packaged in several different configurations. shrink wrapped 4- 5 ounce can pack. flat of 24- 5 ounce individual cans. Shrink wrapped 6- 7 ounce can pack.
- Why it was recalled
- Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum. Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Best By dates: 12/13/2027; 1/13/2028; 01/17/2028; 01/21/2028; 01/23/2028; 01/24/2028; 01/27/2028 Lots: S84N D1N; S84N D2M; S84N 41M; S84N 42M; S84N 42N; S84N 43N; S84N D1L; S84N D3L; S84N D1D; S84N D3D; S84N D2D
- How many
- 14,147 cases total
- Where it was sold
- Product was distributed nationwide.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Feb 4, 2025; FDA classified it on Mar 11, 2025; reported in FDA's enforcement report on Mar 19, 2025.
- FDA recall number
- F-0611-2025
Chicken of the Sea; Thai Union · Mar 19, 2025
- Product
- Genova branded Yellowfin Tuna in Extra Virgin Olive Oil and Sea Salt; NET WT. 5 OZ (142g) RD WT. 4 OZ (113g); Distributed by Tri-Union Seafoods, LLC.; El Sugundo, CA 90245 U.S.A. UPC# 48000 13275
- Why it was recalled
- Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum. Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Best By dates: 01/17/2028 Lots: S88N D1M
- How many
- 14,147 cases total
- Where it was sold
- Product was distributed nationwide.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Feb 4, 2025; FDA classified it on Mar 11, 2025; reported in FDA's enforcement report on Mar 19, 2025.
- FDA recall number
- F-0617-2025
Mutual Trading Company Inc. · Feb 12, 2025
- Product
- Product is individually packaged in opaque airtight plastic packaging with Chinese lettering on one side. Opposite side contains English label that reads: #61122; ANKIMOBO (prepared Monkfish Liver) Ingredients: Monkfish Liver, Brewed Alcohol, (Rice, Rice Malt), Enzyme. CONTAINS: Fish (Monkfish), UPC code: 72546611224 Imported By Mutual Trading Co., Inc.; El Monte, CA 91731 North American Food Dist., Co., Inc.; W. Sacramento, CA 95691; Product of China; NET WT: 7.05 OZ (200 g) "Keep Under Refrigeration"; #16143N
- Why it was recalled
- Imported Monkfish Liver undeclared allergen (Milk) People who are allergic or sensitive to milk run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Two lots: Best By 11/15/2024 Best BY 06/30/2025
- How many
- 70 cases
- Where it was sold
- Firm distributed product in CT, FL, GA, MA, MD, NJ, NY
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 15, 2025; FDA classified it on Feb 6, 2025; reported in FDA's enforcement report on Feb 12, 2025.
- FDA recall number
- F-0534-2025
R. Walters Foods, Limited Liability Corporation · Dec 4, 2024
- Product
- Hannaford brand seafood salad; Net Wt. 12 oz. (340g); INGREDIENTS: SEAFOOD BLEND (FISH PROTEIN [ALASKA POLLOCK AND/OR PACIFIC WHITING], WATER, WHEAT STARCH, SUGAR, SORBITOL, MODIFIED POTATO STARCH, CONTAINS 2% OR LESS OF: NATURAL AND ARTIFICIAL CRAB FLAVORS [SWIMMING CRAB, SNOW CRAB], MIRIN WINE [SAKE, SUGAR, SALT, WATER, YEAST EXTRACT], EGG WHITES, SALT, SOYBEAN OIL, SODIUM TRIPOLYPHOSPHATE, TETRASODIUM PYROPHOSPHATE, CARMINE, PAPRIKA OLEORESIN, COLOR ADDED), MAYONNAISE (SOYBEAN OIL, EGG YOLK, VINEGAR, WATER, SUGAR, SALT, SPICES, NATURAL FLAVOR), CELERY, WATER, NATURAL FLAVORS, MODIFIED FOOD STARCH, NISIN, CITRIC ACID.; CONTAINS: EGGS, WHEAT, ALASKA POLLOCK, PACIFIC WHITING, SWIMMING CRAB, SNOW CRAB; DISTRIBUTED BY: HANNAFORD BROS. CO., LLC; UPC: 0 41268 25161 2
- Why it was recalled
- Product contains undeclared hydrolyzed soy protein. People who are allergic to soy run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- USE By : 11/13/24 and USE By : 11/14/24
- How many
- 278 cases
- Where it was sold
- Maine, New Hampshire, Vermont, Massachusetts, New York.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 29, 2024; FDA classified it on Nov 25, 2024; reported in FDA's enforcement report on Dec 4, 2024.
- FDA recall number
- F-0147-2025
What to do
- Compare the brand, product name, size, UPC and the lot code or best-by date on your package with the recall. Recalls usually cover specific lots or dates, not every package.
- If your product matches, do not eat it. Return it to the store for a refund or throw it away, as the recall notice says.
- If you or someone in your family feels sick after eating a recalled food, call your doctor and say which product it was. Get emergency care for severe symptoms.
- Report a problem or illness to FDA through the Safety Reporting Portal (safetyreporting.hhs.gov). For meat, poultry and egg products, call USDA at 1-888-674-6854.