Par Pharmaceutical, Inc. recalls Mycophenolate Mofetil for Injection, USP 500 mg, 4 Single Dose Vials, Rx Only, Distributed by: Par Pharmaceutical Chest
Recalled May 15, 2019 · FDA recall D-1293-2019 · Par Pharmaceutical
Hazard
Presence of Particulate Matter; glass fragment observed in one vial of reconstituted product · FDA Class I
Units
4506 packs
Sold at
nationwide
Description
Presence of Particulate Matter; glass fragment observed in one vial of reconstituted product
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
Manufacturer(s)
Par Pharmaceutical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →