Class II

Drug Recall: Pemetrexed for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0834-01

Reliance Life Sciences Private Limited · June 24, 2026

Reason for Recall

Lack of Sterility Assurance

Distribution

Nationwide in the USA

States Affected

NATIONWIDE

Quantity Affected

12,000 vials

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0671-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.