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Walmart Inc

Recalls

Recalls by year

A bar chart of the number of recalls naming this company by year.

Recalls by year
YearRecalls
20223
20243
20251
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FDA Recall United States Terminated Historical recordClass I

Walmart Inc

Product
Fresh cut cucumber slices, Marketside, packaged in clear pla…
Reason
Potential Salmonella contamination.
Published
June 11, 2025
Distribution
12 Retail locations in Texas: Ennis, TX;…

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FDA Recall United States Terminated Historical recordClass I

Walmart Inc

Product
Marketside Fresh Cut Cucumber Slices. In clear deli plastic…
Reason
Sliced cucumbers have the potential to be contaminated with Salmonella.
Published
December 18, 2024
Distribution
TX

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FDA Recall United States Terminated Historical recordClass III

Walmart Inc

Product
Great Value Cherry Mixed Fruit, 4 oz, 4 Count and 12 count p…
Reason
FD&C Red No 3 was not declared as an ingredient.
Published
October 23, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Walmart Inc

Product
Great Value Diced Peaches, Mandarin Segments, & Cherry Mixed…
Reason
FD&C Red No 3 was not declared as an ingredient.
Published
October 23, 2024
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, a) 100-count bottles labeled with UPC 7 501031 111190 and UPC 6 09002 40885, and b) 2 pack of 100-count bottles per carton UPC 3 72426 01434

by Walmart Inc

Reason
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
Published
June 22, 2022
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.

by Walmart Inc

Reason
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
Published
June 22, 2022
Distribution
Nationwide

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FDA Recall Completed Historical recordClass I

Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles, Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800, Mexico, D.F., UPC 7 501031 111190.

by Walmart Inc

Reason
Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation.
Published
June 22, 2022
Distribution
Nationwide

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Showing 1–7 of 7 results

This page lists recalls that name Walmart Inc as the recalling firm in the official source notice. It is not a safety rating, ranking, or statement that the company acted negligently. Read the full medical disclaimer.