Class II

Drug Recall: Bortezomib for Injection 3.5mg/Vial, 10 mL per Single-Dose Vial, For Intravenous or Subcutaneous Use, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873. NDC: 70069-0836-01

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

11,400 vials

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0673-2026

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: Bortezomib for Injection 3.5mg/Vial, 10 mL per Single-Dose Vial, For Intravenous or Subcutaneous Use, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873. NDC: 70069-0836-01 | SafeCheck