FDA Drug · D-0672-2026

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

Class II · Ongoing

Lack of Sterility Assurance

Affected lots / codes — check yours against thisLot, expiry: RPTH0125A Jan 31, 2028; RPTH0225A Jan 31, 2028; RPTH0325A Jan 31, 2028; RPTH0725A Apr 30, 2028;

Recalling firm: Reliance Life Sciences Private Limited, Navi Mumbai, N/A
Classification: Class II (temporary or reversible harm possible)
Status: Ongoing
Quantity: 5,020 vials
Distribution: Nationwide in the USA
Recall initiated: June 24, 2026
Classified: July 8, 2026
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0672-2026%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

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