Meijer Steam Distilled Water, 128 FL OZ (1 GAL) 3.78L, packaged in a plastic jug with red plastic lid, UPC 041250841197,
Summary
The FDA issued a Class II for Meijer Steam Distilled Water, 128 FL OZ (1 GAL) 3.78L, packaged in a plastic jug by Meijer Inc. Reason: Floating black foreign substance in the product.
Details
Source
Food Recall
External ID
H-0408-2026
Action Date
2026-01-14
Status
Terminated
Category
food
Product Description
Meijer Steam Distilled Water, 128 FL OZ (1 GAL) 3.78L, packaged in a plastic jug with red plastic lid, UPC 041250841197, Dist. By Meijer Distribution, Inc. Grand Rapids, MI 49544, packed 4 per case
Lot/Code Info: SELL BY OCT 04 2026 Lot Code: 39-222 #3 Product ID (PID): 472859 Meijer Item Code (MIC): 477910
Quantity Affected: 38,043 gallons
Reason for Recall
Floating black foreign substance in the product
Distribution
IL, IN, KY, OH, MI, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2025-11-13
Company
Grand Rapids, MI
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 36 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Meijer Inc has 18 FDA actions in our database, including 18 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 (Meijer Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Meijer Inc have FDA actions?
Meijer Inc has 18 FDA actions in our database, including 18 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0408-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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