Azacitidine for Injection recall: Subpotent
Azacitidine for Injection, 100 mg Lyophilized Powder, Single-Dose Vials, Rx Only, Manufactured by: Intas Pharmaceuticals Limited, Pharmez…
Why was Azacitidine for Injection recalled?
Subpotent Drug
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 #: FE22001A, Exp. Date 01/2024
- Product
- Azacitidine for Injection, 100 mg Lyophilized Powder, Single-Dose Vials, Rx Only, Manufactured by: Intas Pharmaceuticals Limited, Pharmez…
- Recalling firm
- Amerisource Health Services LLC
- Quantity
- 4,160 vials
- Distribution
- Nationwide within the USA
- Recall date
- August 24, 2022
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)