Topo Chico MINERAL WATER CARBONATED 16.9 FL OZ (500mL) Bottle UPC 0 21136 18061 9, Case UPC 0 21136 18062 6 MADE IN MEXI
Summary
The FDA issued a Class II for Topo Chico MINERAL WATER CARBONATED 16.9 FL OZ (500mL) Bottle UPC 0 21136 18061 by The Coca-Cola Company. Reason: Pseudomonas in Mineral Water. The firm was notified by their distributor that product placed on hold was released and shipped to customers..
Details
Source
Food Recall
External ID
H-0048-2025
Action Date
2025-06-25
Status
Completed
Category
food
Product Description
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.
Lot/Code Info: Lot #11 A 2543, Lot #12 A 2543 & Lot #13 A 2541
Quantity Affected: 241cases/18/16.9 oz (500mL)
Reason for Recall
Pseudomonas in Mineral Water. The firm was notified by their distributor that product placed on hold was released and shipped to customers.
Distribution
Product was shipped to the following states: AZ, LA, NM, NV & TX.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-05-28
Company
Atlanta, GA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
The Coca-Cola Company has 7 FDA actions in our database, including 7 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (The Coca-Cola Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The Coca-Cola Company have FDA actions?
The Coca-Cola Company has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0048-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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