Bottled water recalls: brands, lot codes and what to do
Short answer: FDA has listed 10 bottled water recalls reported since November 2024; the most recent was reported on May 6, 2026 (Guangdong Zonegoing Food Co., LTD). 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 10 recalls
Recall details
Guangdong Zonegoing Food Co., LTD · May 6, 2026
- Product
- 52USA brand POPPING BOBA; PASSION FRUIT FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-malic acid (E296), sodium alginate (E401), citric acid (E330), carrageenan (EE407), potassium chloride (E508), potassium sorbate (E202), guar gum (E412), trisodium citrate (E331), beta-carotene (E160a). sucralose (E955), tartrazine (E102), sunset yellow (E110)), food flavors.; CONTAINS NO JUICE; Shelf Life: 18 months; Distributed for Felicific Inc., Queens, NY 11435; PRODUCT OF CHINA; UPC 8 1018 42125 1
- Why it was recalled
- Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).
- 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 Numbers: 20250813 Expiration Date: Feb 8, 2027
- How many
- 5,196 units (total)
- Where it was sold
- NY
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Apr 13, 2026; FDA classified it on Apr 24, 2026; reported in FDA's enforcement report on May 6, 2026.
- FDA recall number
- H-0677-2026
Guangdong Zonegoing Food Co., LTD · May 6, 2026
- Product
- 52USA brand POPPING BOBA; MANGO FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-malic acid (E296), sodium alginate (E401), citric acid (E330), carrageenan (EE407), potassium chloride (E508), potassium sorbate (E202), guar gum (E412), trisodium citrate (E331), beta-carotene (E160a). sucralose (E955), tartrazine (E102), sunset yellow (E110)), food flavors.; CONTAINS NO JUICE; Shelf Life: 18 months; Distributed for Felicific Inc., Queens, NY 11435; PRODUCT OF CHINA; UPC 8 1018 42124 4
- Why it was recalled
- Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).
- 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 Numbers: 20250813 Expiration Date: Feb 8, 2027
- How many
- 5,196 units (total)
- Where it was sold
- NY
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Apr 13, 2026; FDA classified it on Apr 24, 2026; reported in FDA's enforcement report on May 6, 2026.
- FDA recall number
- H-0678-2026
Guangdong Zonegoing Food Co., LTD · May 6, 2026
- Product
- 52USA brand POPPING BOBA; STRAWBERRY FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-malic acid (E296), sodium alginate (E401), citric acid (E330), carageenan (EE407), potassium chloride (E508), potassium sorbate (E202), guar gum (E412), trisodium citrate (E331), sucralose (E955), allura red (E129), food flavors.; CONTAINS NO JUICE; Shelf Life: 18 months; Distributed for Felicific Inc., Queens, NY 11435; PRODUCT OF CHINA; UPC 8 10185 42123 7
- Why it was recalled
- Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).
- 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 Numbers: 20250813 Expiration Date: Feb 8, 2027
- How many
- 5,196 units (total)
- Where it was sold
- NY
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Apr 13, 2026; FDA classified it on Apr 24, 2026; reported in FDA's enforcement report on May 6, 2026.
- FDA recall number
- H-0676-2026
Valley Springs Artesian Gold, LLC · Mar 4, 2026
- Product
- Valley Springs 100% Natural Bottled Water. Fluoride Added. 1 Gal Net, 128 Fl. Oz. UPC 0 31193-01301 0. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901.
- Why it was recalled
- Water was bottled under insanitary conditions.
- 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
- How many
- 7,840 units
- Where it was sold
- IL, WI
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Feb 6, 2026; FDA classified it on Feb 26, 2026; reported in FDA's enforcement report on Mar 4, 2026.
- FDA recall number
- H-0535-2026
Valley Springs Artesian Gold, LLC · Mar 4, 2026
- Product
- Valley Springs 100% Natural Bottled Water packaged in the following size plastic jug with plastic caps: 1. 1 Gal Net 128 Fl oz. UPC 0 31193-00701 9. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901. 2. 2.5 Gallon Net (320 Fl oz./9.4L). UPC 0 31193-01501 4. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901. 3. Infant Water, 1 Gal Net, 128 FL. Oz. Not sterile. Use as directed by physician or by labeling directions for use of infant formula. UPC 0 31193-01401 7. 4. Daisy's Doggy Water, 1 Gal Net, 128 FL. Oz. 100% Pure Water. No Chlorine. UPC 0 31193-90100 3. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901. Distributed by DDW LLC, 109 S. Thompson Rd., Sun Prairie, WI 53590.
- Why it was recalled
- Water was bottled under insanitary conditions.
- 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
- How many
- 379,868 units
- Where it was sold
- IL, WI
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Feb 6, 2026; FDA classified it on Feb 26, 2026; reported in FDA's enforcement report on Mar 4, 2026.
- FDA recall number
- H-0534-2026
3rd Day Beverages LLC · Jul 23, 2025
- Product
- LION Pineapple Spring Water Hydration Drink, 20 fl. oz, packaged in PET bottles, packed 12 per case
- Why it was recalled
- Potential contamination with floating objects
- 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
- UPC/Product Number: 198715474572; Batch Numbers: 25121 through 25128; Best By 05/26
- How many
- 41 cases
- Where it was sold
- Product was distributed to three (3) retailers in: TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jun 11, 2025; FDA classified it on Jul 15, 2025; reported in FDA's enforcement report on Jul 23, 2025.
- FDA recall number
- H-0276-2025
3rd Day Beverages LLC · Jul 23, 2025
- Product
- LION Lemon Lime Spring Water Hydration Drink, 20 fl. oz, packaged in PET bottles, packed 12 per case
- Why it was recalled
- Potential contamination with floating objects
- 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
- UPC/Product Number: 198715712469; Batch Numbers: 25121 through 25128 ; Best By 05/26
- How many
- 58 cases
- Where it was sold
- Product was distributed to three (3) retailers in: TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jun 11, 2025; FDA classified it on Jul 15, 2025; reported in FDA's enforcement report on Jul 23, 2025.
- FDA recall number
- H-0275-2025
3rd Day Beverages LLC · Jul 23, 2025
- Product
- LION Watermelon Spring Water Hydration Drink, 20 fl. oz, packaged in PET bottles, packed 12 per case
- Why it was recalled
- Potential contamination with floating objects
- 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
- UPC/Product Number: 198715104172; Batch Numbers: 25121 through 25128; Best By 05/26
- How many
- 48 cases
- Where it was sold
- Product was distributed to three (3) retailers in: TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jun 11, 2025; FDA classified it on Jul 15, 2025; reported in FDA's enforcement report on Jul 23, 2025.
- FDA recall number
- H-0274-2025
3rd Day Beverages LLC · Jul 23, 2025
- Product
- LION Mixed Berry Spring Water Hydration Drink, 20 fl. oz, packaged in PET bottles, packed 12 per case
- Why it was recalled
- Potential contamination with floating objects
- 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
- UPC/Product Number: 198715525045; Batch Numbers: 25121 through 25128; Best By 05/26
- How many
- 43 cases
- Where it was sold
- Product was distributed to three (3) retailers in: TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jun 11, 2025; FDA classified it on Jul 15, 2025; reported in FDA's enforcement report on Jul 23, 2025.
- FDA recall number
- H-0277-2025
The Coca-Cola Company · Jun 25, 2025
- Product
- Topo Chico MINERAL WATER CARBONATED 16.9 FL OZ (500mL) Bottle UPC 0 21136 18061 9, Case UPC 0 21136 18062 6 MADE IN MEXICO BY: CIA. TOPO CHICO, S. DE R.L. DE C.V. MONTERREY NO. 6500 COL. TOPO CHICO, MTY.
- Why it was recalled
- Pseudomonas in Mineral Water. The firm was notified by their distributor that product placed on hold was released and shipped to customers.
- 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 #11 A 2543, Lot #12 A 2543 & Lot #13 A 2541
- How many
- 241cases/18/16.9 oz (500mL)
- Where it was sold
- Product was shipped to the following states: AZ, LA, NM, NV & TX.
- Status
- Completed: the company has finished its recall actions.
- Dates
- Recall started May 28, 2025; FDA classified it on Jun 17, 2025; reported in FDA's enforcement report on Jun 25, 2025.
- FDA recall number
- H-0048-2025
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.