RecallHawk
Class III Recall

Berkeley Springs Water Purified , Berkeley Springs Water Distilled , One Gallons & Five Gallons, Plastic, 6 gallons in o

Berkeley Club Beverages, Inc.

Summary

The FDA issued a Class III for Berkeley Springs Water Purified , Berkeley Springs Water Distilled , One Gallons by Berkeley Club Beverages, Inc.. Reason: Product tested positive for coliforms..

Details

Source

Food Recall

External ID

F-0123-2025

Action Date

2024-11-20

Status

Terminated

Category

food

Product Description

Berkeley Springs Water Purified , Berkeley Springs Water Distilled , One Gallons & Five Gallons, Plastic, 6 gallons in one case and1 individual 5 Gallon, Codes 090326,090426,090526,090626.

Lot/Code Info: 090326,090426,090526,090626

Quantity Affected: 1304 Bottles

Reason for Recall

Product tested positive for coliforms.

Distribution

Product distributed in West Virgnia, Maryland, Virgnia

Type: Voluntary: Firm initiated

Recall Initiated: 2024-09-12

Company

Berkeley Club Beverages, Inc.

Berkeley Springs, WV

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 38 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III 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 (Berkeley Club Beverages, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Berkeley Club Beverages, Inc. have FDA actions?

This is the only FDA action we have on record for Berkeley Club Beverages, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0123-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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