RecallHawk
Class II Recall

Valley Springs 100% Natural Bottled Water. Fluoride Added. 1 Gal Net, 128 Fl. Oz. UPC 0 31193-01301 0. Bottled by Va

Valley Springs Artesian Gold, LLC

Summary

The FDA issued a Class II for Valley Springs 100% Natural Bottled Water. Fluoride Added. 1 Gal Net, 128 Fl. by Valley Springs Artesian Gold, LLC. Reason: Water was bottled under insanitary conditions..

Details

Source

Food Recall

External ID

H-0535-2026

Action Date

2026-03-04

Status

Ongoing

Category

food

Product Description

Valley Springs 100% Natural Bottled Water. Fluoride Added. 1 Gal Net, 128 Fl. Oz. UPC 0 31193-01301 0. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901.

Lot/Code Info: All Codes

Quantity Affected: 7,840 units

Reason for Recall

Water was bottled under insanitary conditions.

Distribution

IL, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2026-02-06

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 27 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Valley Springs Artesian Gold, LLC has 3 FDA actions in our database, including 3 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 (Valley Springs Artesian Gold, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Valley Springs Artesian Gold, LLC have FDA actions?

Valley Springs Artesian Gold, LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0535-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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