Reliance Life Sciences Private Limited: Pemetrexed For Injection 500mg/vial, 1
Recall Summary Pemetrexed for Injection 500mg/Vial (a cancer medication) manufactured by Reliance Life Sciences and distributed nationwide under the Somerset Therapeutics brand is being recalled because it lacks proper sterility assurance, meaning the product may not be sterile. This is a Class II recall affecting all 50 states and Washington, D.C.
- Recalling firm
- Reliance Life Sciences Private Limited
- Product
- Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0835-01
- Reason
- Lack of Sterility Assurance
- Classification
- Class II
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-06-24
- 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/6250f6d9-c52f-4962-8f2c-55cc9d903317