Opdualag (nivolumab and relatlimab-rmbw) injection, 240 mg and 80 mg/20 mL (12mg and 4mg/mL),Single Dose Vial, RX Only, Bristol-Myers Squibb Company, Princeton, NJ 08543, NDC 0003-7125-11

Recall Number: D-0097-2026

Firm: Bristol-Myers Squibb Company

Classification: Class II

Status: Ongoing

Report Date: 20251029

Initiation Date: 20251021

Termination Date:

Reason for Recall

Lack of Assurance of Sterility.

Product Description

Opdualag (nivolumab and relatlimab-rmbw) injection, 240 mg and 80 mg/20 mL (12mg and 4mg/mL),Single Dose Vial, RX Only, Bristol-Myers Squibb Company, Princeton, NJ 08543, NDC 0003-7125-11