Voriconazole Tablets recall: CGMP Deviations
Voriconazole Tablets, 50 mg, packaged in cartons of 3 blister cards with 10 individual blistered doses (30 Unit Dose per carton), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC 60687-294-21, Unit Dose NDC 60687-294-11.
Why was Voriconazole Tablets recalled?
cGMP Deviations: Received notification from their supplier requesting they perform a recall due to the fact they repackaged the product.
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?
Lot # 1014138, Exp 04/30/2025
- Product
- Voriconazole Tablets, 50 mg, packaged in cartons of 3 blister cards with 10 individual blistered doses (30 Unit Dose per carton), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC 60687-294-21, Unit Dose NDC 60687-294-11.
- Recalling firm
- Amerisource Health Services LLC
- Quantity
- 889 cartons
- Distribution
- USA nationwide.
- Recall date
- April 9, 2025
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)