Walmart Inc: Drug Recall

Recall #D-1159-2022 · 05/24/2022

Class II: Risk

Recall Details

Recall Number: D-1159-2022
Classification: Class II
Product Type: Drug
Recalling Firm: Walmart Inc
Status: Completed
Date Initiated: 05/24/2022
Location: Bentonville, AR, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 1308 bottles total

Reason for Recall

Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.

Product Description

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

Distribution Pattern

Nationwide in the USA.

Other Recalls by Walmart Inc

Class I: Dangerous 05/20/2025

Potential Salmonella contamination.
Class I: Dangerous 11/28/2024

Sliced cucumbers have the potential to be contaminated with Salmonella.
Class III: Low Risk 09/26/2024

FD&C Red No 3 was not declared as an ingredient.
Class III: Low Risk 09/26/2024

FD&C Red No 3 was not declared as an ingredient.
Class II: Risk 05/24/2022

Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.

View all recalls by Walmart Inc →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.