Topo Chico MINERAL WATER CARBONATED 16.9 FL OZ (500mL) Bottle UPC 0 21136 18061 9, Case…
The Coca-Cola Company recalled this product and the FDA reported the enforcement action on 25 June 2025 as Class II. The recall was initiated by the firm. Pseudomonas in Mineral Water. The firm was notified by their distributor that product placed on hold was released and shipped to customers.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- 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.
- UPC
- 021136180619
- 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.
- Recalling firm
- The Coca-Cola Company
- Firm location
- Atlanta, Georgia, United States
- Classification
- Class II
- Status
- Completed
- Recall number
- H-0048-2025
- Quantity
- 241cases/18/16.9 oz (500mL)
- Distribution
- Product was shipped to the following states: AZ, LA, NM, NV & TX.
- Initiated
- 28 May 2025
- Reported by FDA
- 25 June 2025
- Firm notified by
- Product codes
- Lot #11 A 2543, Lot #12 A 2543 & Lot #13 A 2541
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
- The distribution pattern names 2 states, and the FDA published the enforcement report 4 weeks after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Named in the distribution pattern: Louisiana, New Mexico. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Other records from The Coca-Cola Company
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 14 other records name this firm.
All 15 records for The Coca-Cola Company
All 2025 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.