The Coca-Cola Company Topo Chico MINERAL WATER CARBONATED 16.9 FL OZ recall — FDA H-0048-2025
Pseudomonas in Mineral Water. The firm was notified by their distributor that product placed on hold was released and shipped to customers.
Overview of recall records associated with The Coca-Cola Company, including dates, categories and classifications where available.
Classification mix: Class II: 13, Class III: 1.
Pseudomonas in Mineral Water. The firm was notified by their distributor that product placed on hold was released and shipped to customers.
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
May contain foreign object (metal bolt or washer)
May contain foreign object (metal bolt or washer)
May contain foreign object (metal bolt or washer)
Product labeled to be "zero sugar" may contain sugar due to an incorrect label being used.
The firm was notified via a consumer complaint that the product contained a long piece of metal.
The firm was notified via a consumer complaint that the product contained a long piece of metal.
Foreign matter believed to be glass observed in retain samples of product.
There is the potential for a limited quantity of bottles to contain foreign matter in the form of tiny pieces of wire metal fragments.
Due to a potential package design issue, there is the possibility for consumers to be injured when consuming the product from an unevenly opened pouch.
The product contains undeclared aspartame.
This page summarizes recall records in which the official source identifies The Coca-Cola Company as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.