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You are at:Home » Over 38K gallons of bottled water recalled due to ‘foreign substance’
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Over 38K gallons of bottled water recalled due to ‘foreign substance’

Press RoomBy Press RoomJanuary 16, 2026No Comments2 Mins Read
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Over 38K gallons of bottled water recalled due to ‘foreign substance’
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Tens of thousands of gallons of water bottles distributed to several states are being recalled after officials discovered a floating black foreign substance in the product.

The recall involved 38,043 gallons of its Meijer Steam Distilled Water, which were sold in 128 fluid-ounce (1 gallon) plastic jugs with red plastic lids and distributed across Illinois, Indiana, Kentucky, Ohio, Michigan and Wisconsin, according to a notice posted by the Food and Drug Administration (FDA). 

Michigan-based Meijer Distribution Inc. distributed the products in cases of four. The sell-by date is Oct. 4, 2026, and the product’s lot code is 39-222 #3. 

45 SICKENED WITH SALMONELLA IN CONNECTION WITH RECALL OF SUPER GREENS DIET SUPPLEMENT POWDER

Meijer voluntarily initiated the recall in November 2025. However, officials are continuing to review the issue.

A man is drinking out of a stainless steal water bottle.

The company didn’t release any further details regarding the recall, including how the foreign object was discovered, what the actual substance was and if there were any incidents related to this recall. 

RECALL OF CHEESE PRODUCTS UPGRADED TO HIGHEST DANGER LEVEL OVER LISTERIA-CAUSING BACTERIA: FDA

The FDA didn’t assign a recall classification, either, which indicates how serious the health risk is to consumers. There are three levels. 

Class I is defined as a situation in which there is a reasonable probability that the use of, or exposure to, the product will cause serious adverse health consequences or death. 

A sign for the Food And Drug Administration is seen outside of the headquarters

Class II is when the FDA believes the use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

Class III is when the FDA believes the use of or exposure to a product is not likely to cause adverse health consequences.

Read the full article here

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