Class II

Drug Recall: 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

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

5,020 vials

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0672-2026

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.

Reliance Life Sciences Private Limited Drug Recall: 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 | SafeCheck