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Class IICompleted in FDA datasetRecall initiated May 28, 2025

Topo Chico MINERAL WATER CARBONATED 16.9 FL OZ (500mL) Bottle

Recalling firm: The Coca-Cola Company

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.

Historical recall record. This is not a new recall announcement. “Completed” describes the FDA recall process; it does not certify that an individual package is safe.

Check your package

Compare the exact product and package details with the label you have.

ProductTopo 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.
Package size16.9 FL OZ
UPC021136180619, 021136180626

FDA code information

Lot #11 A 2543, Lot #12 A 2543 & Lot #13 A 2541

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Full FDA record and distribution details

Original 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.

Extracted codes and context

TypeCode / valueContext
UPC021136180619Topo 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, MT
UPC021136180626INERAL 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.

Original FDA recall reason

Pseudomonas in Mineral Water. The firm was notified by their distributor that product placed on hold was released and shipped to customers.

Recall details

Recall number
H-0048-2025
Event ID
96980
FDA status
Completed
Initiated
May 28, 2025
Reported
Jun 25, 2025
Classified
Jun 17, 2025
Quantity
241cases/18/16.9 oz (500mL)
Location
Atlanta, GA, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

Product was shipped to the following states: AZ, LA, NM, NV & TX.

FDA source record · H-0048-2025

Data updated September 16, 2026. View official FDA data ↗

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