Peaches recalls: brands, lot codes and what to do
Short answer: FDA has listed 28 peaches 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 28 recalls
Recall details
El Ruisenor De Mexico, Inc. · Oct 28, 2026
- Product
- Dried Peaches; packed in a clear plastic 1lb, 5lb, 22-25lb unit sizes. No UPC
- Why it was recalled
- undeclared allergen ingredient (Sulfites)
- 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
- 29 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-0118-2027
El Ruisenor De Mexico, Inc. · Oct 28, 2026
- Product
- Jovy Gummy Peach Rings; packed in a clear plastic 1lb unit sizes. UPC: 712199083404
- Why it was recalled
- undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6)
- 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: 6124
- How many
- 687 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-0125-2027
Sempio Food Services, Inc · Oct 28, 2026
- Product
- Sempio Yellow Peach; Product of Korea; NET WT. 14.10 oz. UPC: 8801005320825
- Why it was recalled
- elevated level of lead in canned peaches Lead is toxic. Exposure can cause serious health effects, especially in children.
- 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 code: 2026 06 01 (10:09)
- How many
- 150 cases
- Where it was sold
- Product was primarily distributed to Asian grocery stores in California, Washington, Nevada, Arizona, Hawaii, New Jersey, Georgia, Maryland, New York, Illinois, and Virginia.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Sep 24, 2026; FDA classified it on Oct 19, 2026; reported in FDA's enforcement report on Oct 28, 2026.
- FDA recall number
- H-0102-2027
Joy Gourmet Foods LLC. · Jul 1, 2026
- Product
- Joy Peach Lassi 16 oz.
- Why it was recalled
- Product not adequately pasteurized
- 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
- Expiry June 30 through July 30, 2026 UPC Codes:68061710001
- How many
- 50 gallons (total)
- Where it was sold
- NY, NJ, PA
- Status
- Completed: the company has finished its recall actions.
- Dates
- Recall started Apr 23, 2026; FDA classified it on Jun 23, 2026; reported in FDA's enforcement report on Jul 1, 2026.
- FDA recall number
- H-1092-2026
Albertsons Companies LLC · Jun 10, 2026
- Product
- UPC 25688000000 PIE PEACH MELBA 9IN 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 Almond
- 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
- 7 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-1033-2026
Pocas International Corp. · Apr 8, 2026
- Product
- POPPING BOBA RTD PEACH OOLONG TEA 12 X 13.8OZ
- Why it was recalled
- Packaging integrity issue that may compromise product quality .
- 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
- Will be provided by firm
- How many
- 370 Cases
- Where it was sold
- The product was distributed to the following states: NY, VA, FL, MA, TX, LA, UT, CA and Canada
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Mar 16, 2026; FDA classified it on Mar 27, 2026; reported in FDA's enforcement report on Apr 8, 2026.
- FDA recall number
- H-0633-2026
Moonlight Packing Corporation · Dec 17, 2025
- Product
- Sticker label (for Loose Bulk - peppermint peaches): 4401
- Why it was recalled
- Potential contamination with Listeria monocytogenes. 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
- Lots: 01PCLC, 03PCAF, 106PCLF, 113PCAF, 113PCLF, 129PCLF, 134PCLF, 142PCLF, 150PCLF, 151PCLF, 159PCABA, 159PCABB, 159PCPG10, 20, 22PCAB, 22PCPG10A, 22PCPG10B, 22PCP8A, 22PCPG8B, 22PCPG8C, 23, 25, 30PCEN, 40LT, 40YP#3, 44PCLC, 44PCLCB, 45, 51PCLC, 51PCLCB, 86PCAF, 69PWPR, 79PWPRT
- How many
- 2,622 cases (20 lbs/case)
- Where it was sold
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY Foreign: Canada, Mexico
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 28, 2025; FDA classified it on Dec 17, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0324-2026
Moonlight Packing Corporation · Dec 17, 2025
- Product
- UPC 8 98429 00266 4 Peppermint Peach PROUCE OF U.S.A. 4 COUNT MIN. WT. 2.25 LBS MOONLIGHT PACKING CORPORATION REEDLEY, CA 93654
- Why it was recalled
- Potential contamination with Listeria monocytogenes. 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
- Lots: 01PCLC, 03PCAF, 106PCLF, 113PCAF, 113PCLF, 129PCLF, 134PCLF, 142PCLF, 150PCLF, 151PCLF, 159PCABA, 159PCABB, 159PCPG10, 20, 22PCAB, 22PCPG10A, 22PCPG10B, 22PCP8A, 22PCPG8B, 22PCPG8C, 23, 25, 30PCEN, 40LT, 40YP#3, 44PCLC, 44PCLCB, 45, 51PCLC, 51PCLCB, 86PCAF, 69PWPR, 79PWPRT
- How many
- 439 bags (8-2.25 lb. packs/case)
- Where it was sold
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY Foreign: Canada, Mexico
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 28, 2025; FDA classified it on Dec 17, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0319-2026
Moonlight Packing Corporation · Dec 17, 2025
- Product
- UPC 8 10248 03087 1 Peppermint Peach WHITE PEACHES READY TO EAT FROM CALIFORNIA PRODUCE OF U.S.A. NET WT. 4 LBS. MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654 UPC 8 10248 03163 2 Peppermint Peaches WHITE PEACHES READY TO EAT FROM CALIFORNIA PRODUCE OF U.S.A. NET WT. 4 LBS. MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654
- Why it was recalled
- Potential contamination with Listeria monocytogenes. 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
- Lots: 01PCLC, 03PCAF, 106PCLF, 113PCAF, 113PCLF, 129PCLF, 134PCLF, 142PCLF, 150PCLF, 151PCLF, 159PCABA, 159PCABB, 159PCPG10, 20, 22PCAB, 22PCPG10A, 22PCPG10B, 22PCP8A, 22PCPG8B, 22PCPG8C, 23, 25, 30PCEN, 40LT, 40YP#3, 44PCLC, 44PCLCB, 45, 51PCLC, 51PCLCB, 86PCAF, 69PWPR, 79PWPRT
- How many
- 13,069 cases (4 lbs. / case)
- Where it was sold
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY Foreign: Canada, Mexico
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 28, 2025; FDA classified it on Dec 17, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0315-2026
Moonlight Packing Corporation · Dec 17, 2025
- Product
- UPC 8 98429 00209 1 PEACHES PRODUCE OF U.S.A. NET WT 2 LB (32 OZ) 907 g DISTRIBUTED BY MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654 UPC 0 11110 18174 9 PEACHES PRODUCE OF USA NET WT 32 OZ (2 LB) 907g DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202
- Why it was recalled
- Potential contamination with Listeria monocytogenes. 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
- Lots: 01PCLC, 03PCAF, 106PCLF, 113PCAF, 113PCLF, 129PCLF, 134PCLF, 142PCLF, 150PCLF, 151PCLF, 159PCABA, 159PCABB, 159PCPG10, 20, 22PCAB, 22PCPG10A, 22PCPG10B, 22PCP8A, 22PCPG8B, 22PCPG8C, 23, 25, 30PCEN, 40LT, 40YP#3, 44PCLC, 44PCLCB, 45, 51PCLC, 51PCLCB, 86PCAF, 69PWPR, 79PWPRT
- How many
- 46,048 cases (12-2 lb. bags/case)
- Where it was sold
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY Foreign: Canada, Mexico
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 28, 2025; FDA classified it on Dec 17, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0316-2026
Moonlight Packing Corporation · Dec 17, 2025
- Product
- UPC 8 10248 03186 1 WHITE PEACHES CALIFORNIA FRUIT PRODUCE OF U.S.A. NET WT. 2 LBS. (907G) MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654
- Why it was recalled
- Potential contamination with Listeria monocytogenes. 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
- Lots: 01PCLC, 03PCAF, 106PCLF, 113PCAF, 113PCLF, 129PCLF, 134PCLF, 142PCLF, 150PCLF, 151PCLF, 159PCABA, 159PCABB, 159PCPG10, 20, 22PCAB, 22PCPG10A, 22PCPG10B, 22PCP8A, 22PCPG8B, 22PCPG8C, 23, 25, 30PCEN, 40LT, 40YP#3, 44PCLC, 44PCLCB, 45, 51PCLC, 51PCLCB, 86PCAF, 69PWPR, 79PWPRT
- How many
- 104 cases (12-2 lb. bags/case)
- Where it was sold
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY Foreign: Canada, Mexico
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 28, 2025; FDA classified it on Dec 17, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0317-2026
Moonlight Packing Corporation · Dec 17, 2025
- Product
- Sticker label (for Loose Bulk - white peaches): 4401
- Why it was recalled
- Potential contamination with Listeria monocytogenes. 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
- Lots: 01PCLC, 03PCAF, 106PCLF, 113PCAF, 113PCLF, 129PCLF, 134PCLF, 142PCLF, 150PCLF, 151PCLF, 159PCABA, 159PCABB, 159PCPG10, 20, 22PCAB, 22PCPG10A, 22PCPG10B, 22PCP8A, 22PCPG8B, 22PCPG8C, 23, 25, 30PCEN, 40LT, 40YP#3, 44PCLC, 44PCLCB, 45, 51PCLC, 51PCLCB, 86PCAF, 69PWPR, 79PWPRT
- How many
- 2,375 cases (20 lbs/case)
- Where it was sold
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY Foreign: Canada, Mexico
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 28, 2025; FDA classified it on Dec 17, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0322-2026
Moonlight Packing Corporation · Dec 17, 2025
- Product
- UPC 8 10248 03165 6 YELLOW Peaches PRODUCE OF U.S.A. NET WT. 4 LBS. MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654 UPC 8 98429 00220 6 YELLOW Peaches from California PRODUCE OF U.S.A. NET WT. 4 LBS. MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654
- Why it was recalled
- Potential contamination with Listeria monocytogenes. 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
- Lots: 01PCLC, 03PCAF, 106PCLF, 113PCAF, 113PCLF, 129PCLF, 134PCLF, 142PCLF, 150PCLF, 151PCLF, 159PCABA, 159PCABB, 159PCPG10, 20, 22PCAB, 22PCPG10A, 22PCPG10B, 22PCP8A, 22PCPG8B, 22PCPG8C, 23, 25, 30PCEN, 40LT, 40YP#3, 44PCLC, 44PCLCB, 45, 51PCLC, 51PCLCB, 86PCAF, 69PWPR, 79PWPRT
- How many
- 483,973 cases (4 lbs. / case)
- Where it was sold
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY Foreign: Canada, Mexico
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 28, 2025; FDA classified it on Dec 17, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0314-2026
Moonlight Packing Corporation · Dec 17, 2025
- Product
- Sticker label (for Loose Bulk - yellow peaches): 4044
- Why it was recalled
- Potential contamination with Listeria monocytogenes. 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
- Lots: 01PCLC, 03PCAF, 106PCLF, 113PCAF, 113PCLF, 129PCLF, 134PCLF, 142PCLF, 150PCLF, 151PCLF, 159PCABA, 159PCABB, 159PCPG10, 20, 22PCAB, 22PCPG10A, 22PCPG10B, 22PCP8A, 22PCPG8B, 22PCPG8C, 23, 25, 30PCEN, 40LT, 40YP#3, 44PCLC, 44PCLCB, 45, 51PCLC, 51PCLCB, 86PCAF, 69PWPR, 79PWPRT
- How many
- 237,656 cases (20 lbs/case)
- Where it was sold
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY Foreign: Canada, Mexico
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 28, 2025; FDA classified it on Dec 17, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0320-2026
Moonlight Packing Corporation · Dec 17, 2025
- Product
- Sticker label (for Loose Bulk - peppermint peaches): 4401
- Why it was recalled
- Potential contamination with Listeria monocytogenes. 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
- Lots: 01PCLC, 03PCAF, 106PCLF, 113PCAF, 113PCLF, 129PCLF, 134PCLF, 142PCLF, 150PCLF, 151PCLF, 159PCABA, 159PCABB, 159PCPG10, 20, 22PCAB, 22PCPG10A, 22PCPG10B, 22PCP8A, 22PCPG8B, 22PCPG8C, 23, 25, 30PCEN, 40LT, 40YP#3, 44PCLC, 44PCLCB, 45, 51PCLC, 51PCLCB, 86PCAF, 69PWPR, 79PWPRT
- How many
- 2,603 cases (20 lbs/case)
- Where it was sold
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY Foreign: Canada, Mexico
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 28, 2025; FDA classified it on Dec 17, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0323-2026
Moonlight Packing Corporation · Dec 17, 2025
- Product
- UPC 8 10248 03186 1 Peppermint Peach PRODUCE OF U.S.A. NET WT. 2 LBS. (907G) MOONLIGHT PACKING CORPORATION REEDLEY, CA 93654
- Why it was recalled
- Potential contamination with Listeria monocytogenes. 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
- Lots: 01PCLC, 03PCAF, 106PCLF, 113PCAF, 113PCLF, 129PCLF, 134PCLF, 142PCLF, 150PCLF, 151PCLF, 159PCABA, 159PCABB, 159PCPG10, 20, 22PCAB, 22PCPG10A, 22PCPG10B, 22PCP8A, 22PCPG8B, 22PCPG8C, 23, 25, 30PCEN, 40LT, 40YP#3, 44PCLC, 44PCLCB, 45, 51PCLC, 51PCLCB, 86PCAF, 69PWPR, 79PWPRT
- How many
- 570 cases (12-2 lb. bags/case)
- Where it was sold
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY Foreign: Canada, Mexico
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 28, 2025; FDA classified it on Dec 17, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0318-2026
Moonlight Packing Corporation · Dec 17, 2025
- Product
- Sticker label (for Loose Bulk - yellow peaches): 4044
- Why it was recalled
- Potential contamination with Listeria monocytogenes. 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
- Lots: 01PCLC, 03PCAF, 106PCLF, 113PCAF, 113PCLF, 129PCLF, 134PCLF, 142PCLF, 150PCLF, 151PCLF, 159PCABA, 159PCABB, 159PCPG10, 20, 22PCAB, 22PCPG10A, 22PCPG10B, 22PCP8A, 22PCPG8B, 22PCPG8C, 23, 25, 30PCEN, 40LT, 40YP#3, 44PCLC, 44PCLCB, 45, 51PCLC, 51PCLCB, 86PCAF, 69PWPR, 79PWPRT
- How many
- 102,455 cases (20 lbs/case)
- Where it was sold
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY Foreign: Canada, Mexico
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 28, 2025; FDA classified it on Dec 17, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0321-2026
JFE FRANCHISING INC · Nov 19, 2025
- Product
- Peach Salsa - $5.99-16 oz 639123940636 packaged in clear plastic clamshells Sell by 11/3/2025 Sell by 11/4/2025
- Why it was recalled
- Peaches provided by Moonlight Peaches potentially contaminated with Listeria. 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
- Lots: CBMA341 DAL065 KH366 LV376 CBMA388 DAL088 KH367 LV394 CBMA506 DAL091 KH371 LV396 CBMA512 DAL096 KH389 LV397 CBMA593 DAL302 KH733 LV402 CBMA617 DAL318 KH738 LV713 CBMA819 DAL319 KH739 LV714 CBMA847 FM156 KH748 LV717 CBMA851 FM286 KMA209 LV718 CBMA881 FRYS615 KMA316 LV729 CBMA920 FRYS667 KMA334 LV734 CDMA411 FRYS698 KMA359 LV739 CDMA426 KD213 KMA401 LV744 CDMA435 KD546 KMA402 LV764 CDMA439 KD576 KMA504 LV776 CDMA468 KD584 KMA525 LV779 CDMA475 KD585 KMA554 LV785 CDMA482 KD594 KMA772 MI419 CDMA492 KD596 KS011 MI441 CDMA741 KD689 KS033 MI487 CDMA754 KH115 KS079 MI670 CDMA765 KH128 KS085 MI685 CDMA808 KH136 KS104 MI704 CDMA811 KH138 KS105 MI706 CDMA817 KH144 KS117 NAS526 CDMA836 KH146 KS118 NAS529 CDMA902 KH161 LV008 NAS570 CDMA923 KH179 LV014 NAS582 CDMA945 KH190 LV087 NAS628 CDMA951 KH307 LV224 NAS851 DAL015 KH308 LV292 NAS894 DAL034 KH310 LV339 SM030 DAL049 KH318 LV347 SM131 DAL054 KH346 LV352 SM136 DAL056 KH362 LV356 SM147 DAL061 KH363 LV371 SM475
- How many
- 177 units/ 154.88lbs
- Where it was sold
- AL, AZ, CO, ID, IL, IN, KS, KY, MI, NE, OH, TN, TX, UT, VA, WA, WV, WY
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 29, 2025; FDA classified it on Nov 19, 2025; reported in FDA's enforcement report on Nov 19, 2025.
- FDA recall number
- H-0200-2026
GBC Food Services, LLC · Nov 19, 2025
- Product
- Peach Salsa; UPC 85006540364 14oz (397g); Use by 10/12/2025 to 10/29/2025
- Why it was recalled
- Peaches provided by Moonlight Peaches potentially contaminated with Listeria. 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
- Use by 10/12/2025 to 10/29/2025
- How many
- 154.88 lbs
- Where it was sold
- IL, CO, GA, WA, IN, MS, TN, AR, OR, MI.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 29, 2025; FDA classified it on Nov 19, 2025; reported in FDA's enforcement report on Nov 19, 2025.
- FDA recall number
- H-0199-2026
Pacific Coast Producers · Oct 22, 2025
- Product
- Fruit Cocktail IN 100% JUICE WITH ADDED INGREDIENTS; NET WT 15 OZ (425 g); Ingredients: Diced Peaches, Diced Pears, Water, Grapes, Peach Pulp and Juice, Pineapple Sectors, Pear Juice Concentrate, Halved Cherries (colored red with Carmine), Ascorbic Acid (to protect color).; Distributed By: Wegmans Food Markets, Inc. Rochester, NY 14603
- Why it was recalled
- Potential contamination with heavy metal (Lead). Pieces of foreign material in food can cause injuries such as cuts to the mouth or choking.
- 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: 6FCB 02 C2206 UPC: 077890461525 BEST IF USED BY SEP 01 2027
- How many
- 609 cases (24 cans/case)
- Where it was sold
- U.S. distribution: AL, AR, AZ, CA, FL, GA, IL, IN, KY, LA, ME, MO, MS, NE, NM, NV, NY, OH, OK, PA, SC, TX, UT, VA, WA, WI, WY
- Status
- Completed: the company has finished its recall actions.
- 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-0038-2026
Gina Marie Bakery LLC · Oct 8, 2025
- Product
- Vanilla Cookies with Raspberry Peach Jam
- Why it was recalled
- Undeclared Red 3 and Blue 1
- 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
- UPC Code 757808003169
- How many
- 172 cases (20 containers per case) [total]
- Where it was sold
- Firm notified FDA of recall initiated by state of CT on 09/10/25. A copy of CT press release was requested for posting by FDA. Firm notified customers on 09/11/25.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Sep 10, 2025; FDA classified it on Oct 2, 2025; reported in FDA's enforcement report on Oct 8, 2025.
- FDA recall number
- H-0008-2026
Hi-Tech Pharmaceuticals Inc. · Sep 24, 2025
- Product
- PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT PEACH MANGO NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUPPLEMENT UPC 6 38302 40906 3 Manufactured by: Prime Nutrition 6015-B Unity Drive Norcross, GA 30071
- Why it was recalled
- Unapproved Drug Claims and Misbranded.
- 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 202140114 Exp Date 03/27
- 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-0600-2025
Hillside Orchard Farms Inc. · Aug 27, 2025
- Product
- Fresh Peach Bread Net Wt. 23 oz (652 G) CONTAINS: MILK, SOY, & WHEAT. HILLSIDE ORCHARD FARMS 105 Mitcham Circle, Tiger GA 30576
- Why it was recalled
- 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
- Product #1002 Lot 24323-25197
- How many
- 356cs/12/23oz packages
- Where it was sold
- Product was shipped to the following states: AL, GA, NC, PA & SC.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jul 22, 2025; FDA classified it on Aug 20, 2025; reported in FDA's enforcement report on Aug 27, 2025.
- FDA recall number
- H-0516-2025
Hillside Orchard Farms Inc. · Aug 27, 2025
- Product
- Peach Fritter Net Weight 7 oz (198g) CONTAINS: Wheat, Soybeans, & Milk. Made By: Hillside Orchard Farms 105 Mitcham Circle Tiger, GA 30576
- Why it was recalled
- 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
- Product #1052 Lot 24323-25197
- How many
- 214cs/25/7oz unit
- Where it was sold
- Product was shipped to the following states: AL, GA, NC, PA & SC.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jul 22, 2025; FDA classified it on Aug 20, 2025; reported in FDA's enforcement report on Aug 27, 2025.
- FDA recall number
- H-0517-2025
Dollar General Corporation · Aug 13, 2025
- Product
- Yoplait Original Harvest Peach Yogurt, 6 OZ (170g), packaged in a plastic cup, UPC: 170470003075
- Why it was recalled
- Temperature abuse due to temperature excursion in one shipping trailer
- 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
- Exact lot codes/expiration dates are unknown.
- How many
- 1 eaches
- Where it was sold
- LA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jul 14, 2025; FDA classified it on Aug 6, 2025; reported in FDA's enforcement report on Aug 13, 2025.
- FDA recall number
- H-0417-2025
Knockroe Inc · May 21, 2025
- Product
- Bonya Peach Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
- Why it was recalled
- Undeclared Almonds People who are allergic to tree nuts 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
- Pallet Lot #s: 112, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179,180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202,203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216
- How many
- 9426 Units
- Where it was sold
- The recalled product was distributed to the following states: NY, PA, MA, NJ.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Mar 29, 2025; FDA classified it on May 9, 2025; reported in FDA's enforcement report on May 21, 2025.
- FDA recall number
- F-0767-2025
Vidaslim Co. · Feb 12, 2025
- Product
- VidaSlim 90-day (Original Root, Root Plus, and Root Capsules), VidaSlim 30-day (Original Root, Root Plus, and Root Capsules), VidaSlim 7-day Sample Size (Original Root, Root Plus, and Root Capsules), and VidaSlim Hot Body Brew (Strawberry and Peach flavors),
- Why it was recalled
- Due to the presence of Toxic yellow oleander
- 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 12/24 (December 2024) through 12/25 (December 2025)
- How many
- 760 units
- Where it was sold
- These products were sold on a website and through direct sales via independent distributors throughout the USA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Dec 11, 2024; FDA classified it on Feb 3, 2025; reported in FDA's enforcement report on Feb 12, 2025.
- FDA recall number
- F-0468-2025
The Mochi Ice Cream Company · Feb 5, 2025
- Product
- My Mochi Sorbet Peach Mango Sorbet; Keep Frozen; 6 pieces per container; 6-1.25 OZ (35g) PIECES NET WT 7.5 OZ (210g)*** Nutritional Panel: 6 servings per container; JOYFULLY CHILL!; Made in a nut-free facility; Made by My/Mochi, 5563 Alcoa Ave., Los Angeles, CA 90058; www.mymochi.com; Plant No. 06-00024, EU# 3009013677; Product of USA; UPC# 0-70934-99868-1; Affected lots (Lot# 337-24; Lot#341-24)
- Why it was recalled
- Frozen Peach Mango Sorbet contains undeclared allergen (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
- USE by: 12/2/2025 and 12/6/2025
- How many
- 1350 cases
- Where it was sold
- Product was distributed nationwide. No foreign distribution.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 6, 2025; FDA classified it on Jan 28, 2025; reported in FDA's enforcement report on Feb 5, 2025.
- FDA recall number
- F-0431-2025
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.