Food, drugs, devices › The Coca-Cola Company
Food recall: 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
FDA enforcement event 96980 is a food recall by The Coca-Cola Company of Atlanta, GA, initiated 28 May 2025 and classified Class II, with 1 product record.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 54% of the 569 food enforcement events initiated in 2025 carry the same class.
Status: Completed. Initiation: voluntary: firm initiated. The Coca-Cola Company has 10 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
The Coca-Cola Company, Atlanta, GA.
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."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| H-0048-2025 | 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. | 241cases/18/16.9 oz (500mL) | Class II | Completed | 25 Jun 2025 |
Context
Other enforcement events for The Coca-Cola Company
All 10 events for The Coca-Cola Company
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Pseudomonas in Mineral Water. The firm was notified by their distributor that product placed on hold was released and shipped to customers."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "Product was shipped to the following states: AZ, LA, NM, NV & TX."
Is the recall still ongoing?
FDA lists the status as Completed. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.