Artri Ajo King Tablets Recalled for Unapproved Drug Claims
Walmart is recalling all lots of Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets nationwide. The product was marketed without FDA approval based on unapproved labeling claims.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class II recall involving labeling non-compliance and unapproved drug claims. No reported illnesses, injuries, or hospitalization are documented. The hazard is regulatory non-compliance rather than a specific product safety defect.
Plain-English summary
Walmart Inc. is recalling all lots of Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, 100-count bottles (UPC 7 501031 12705), distributed nationwide in the USA. The recall involves 1,308 bottles total.
The FDA found that all lots of this product were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). The product was classified as an unapproved drug based on its labeling claims.
Consumers who have purchased this product should discontinue use and discard it. Anyone who has taken this product and has concerns should contact their healthcare provider.
The recalled product
- Product
- Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.
- Manufacturer
- Walmart Inc
- Category
- Drug
- Affected units
- 1,308
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All product lots.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 3 recalled by Walmart Inc under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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