FDA recall D-0672-2026

Reliance Life Sciences Private Limited · Class II · drug

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

Distribution

Nationwide in the USA

Key facts

Status: Ongoing
Initiation date: 2026-06-24
Report date: 2026-07-15
Voluntary/Mandated: Voluntary: Firm initiated
Location: Navi Mumbai, N/A, India

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0672-2026