Mycophenolate Mofetil for Injection recall: Particulate Matter
Mycophenolate Mofetil for Injection, USP 500 mg, 4 Single Dose Vials, Rx Only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977 NDC 342023-172-044
Why was Mycophenolate Mofetil for Injection recalled?
Presence of Particulate Matter; glass fragment observed in one vial of reconstituted 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?
AD812, exp 9/2020
- Product
- Mycophenolate Mofetil for Injection, USP 500 mg, 4 Single Dose Vials, Rx Only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977 NDC 342023-172-044
- Recalling firm
- Par Pharmaceutical, Inc.
- Quantity
- 4506 packs
- Distribution
- nationwide
- Recall date
- May 15, 2019
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)