Drug recall D-0672-2026

Class II Ongoing reported Jul 15, 2026

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 for recall

Lack of Sterility Assurance

Lots and codes

Lot, expiry: RPTH0125A Jan 31, 2028; RPTH0225A Jan 31, 2028; RPTH0325A Jan 31, 2028; RPTH0725A Apr 30, 2028;

Recall details

Recalling firm
Reliance Life Sciences Private Limited, Navi Mumbai, N/A
Quantity
5,020 vials
Distribution
Nationwide in the USA
Type
Voluntary: Firm initiated
Recall initiated
June 24, 2026