RecallHawk

Gerolsteiner 750ml Sparkling Water Bottles

Gerolsteiner Brunnen GmbH & Co. KG, of Germany

Summary

CPSC recall: Gerolsteiner 750ml Sparkling Water Bottles. By Gerolsteiner Brunnen GmbH & Co. KG, of Germany. Hazard: The recalled water bottles can crack, causing a laceration hazard.. Remedy: Consumers should immediately stop using the recalled Gerolsteiner sparkling water bottles, and return the bottles from the affected lots to the store where they were purchased for a full refund. Consumers will not be asked for proof of purchase, but will need to return the recalled bottle to receive a refun

Details

Source

CPSC Consumer Product Recall

External ID

10202

Action Date

2025-03-13

Status

Recalled

Category

consumer_product

Product Description

This recall involves Gerolsteiner 750ml sparkling water bottles from two specific lots. The water was sold in large 750m

Context & Analysis

This is a unclassified recall.

This was one of 15 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Gerolsteiner Brunnen GmbH & Co. KG, of Germany has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Gerolsteiner Brunnen GmbH & Co. KG, of Germany) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Gerolsteiner Brunnen GmbH & Co. KG, of Germany have FDA actions?

Gerolsteiner Brunnen GmbH & Co. KG, of Germany has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10202" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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