Walmart recalls 100-count Artri Ajo King Reforzado tablets with unapproved labeling claims. Consumers should check UPC 7 501031 12705 for affected lots.
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
Walmart is recalling 100-count Artri Ajo King Reforzado tablets that were marketed without proper FDA approval. This is a regulatory issue, not a safety hazard for consumers.
The product was sold without FDA approval, meaning it does not meet regulatory standards for drug labeling. This is a legal issue, not a direct health risk to consumers.
Anyone who purchased the original 100-count bottles of Artri Ajo King Reforzado tablets with UPC 7 501031 12705 from Walmart. The risk is low as this is a regulatory issue, not a safety hazard.
Check for the UPC 7 501031 12705 on the product label. The affected items are 100-count bottles of Artri Ajo King Reforzado tablets sold by Walmart.
Look for the UPC 7 501031 12705 on the bottle to confirm if it's affected.
The recall is due to regulatory labeling issues, not a safety hazard. The product is not unsafe for use but is unapproved by the FDA.
Check for the UPC 7 501031 12705 on the 100-count bottle label.
The recall does not require immediate action beyond checking the label. No specific remedy is provided.
We’ve drafted a message you can send Walmart to request your refund or repair — edit it as you like.
Subject: Recall D-1158-2022 — Walmart Walmart Hello, I own a Walmart that is covered by recall D-1158-2022 from Walmart. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
