US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jul 29, 2026 (35 days ago)

SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

What was recalled

SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-811-02

Recalling firm
Apollo Care, LLC
NDC code
71170-811-02
Origin
MO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0748-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Semaglutide recalls

See all