Artri Ajo King recall: Labeling Error
Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.
Why was Artri Ajo King recalled?
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All product lots.
- Product
- Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.
- Recalling firm
- Walmart Inc
- Quantity
- 1308 bottles total
- Distribution
- Nationwide in the USA.
- Recall date
- June 22, 2022
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (drug)