FDAFDA · Food and drugs·Recall number D-1293-2019
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
Published May 15, 2019 · Recall initiated: April 30, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Particulate Matter; glass fragment observed in one vial of reconstituted product
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- MYCOPHENOLATE MOFETIL
- Manufacturer
- Par Pharmaceutical, Inc.
- Distributor
- nationwide
- UPC
- 342023172044
- Lot
- AD812, exp 9/2020
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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