Shilpa Medicare Limited: Pemrydi Rtu(pemetrexed Injection), 500 Mg/50 Ml (10 Mg/ml), Single-dose Vial
PEMRYDI RTU Recall Summary Shilpa Medicare is recalling PEMRYDI RTU (pemetrexed injection) 500 mg vials distributed nationwide because some vials contain green to dark green discoloration in the solution. The affected product was manufactured by Zydus Lifesciences and distributed by Amneal Pharmaceuticals. This recall affects patients who received this cancer medication across all U.S. states and Washington, D.C.
- 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/8955c2ef-8b5d-4c07-9c69-c36338c3e746