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