Shilpa Medicare Limited: Pemrydi Rtu(pemetrexed Injection), 500 Mg/50 Ml (10 Mg/ml), Single-dose Vial
- Recalling firm
- Shilpa Medicare Limited
- Product
- PEMRYDI RTU(pemetrexed injection), 500 mg/50 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus Lifesciences Limited, Ahmedabad, India; Distributed by: Amneal Pharmaceuticals LC, Bridgewater, NY 08807. NDC: 70121-2461-1
- Reason
- Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
- Classification
- Class II
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-07-29
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Nationwide in the USA.
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/1fc408dc-cbf9-4cdf-88b9-996d21118611