RecallHawk
Class II 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

The Coca-Cola Company

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

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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