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

SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only…

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 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-722-02

Recalling firm
Apollo Care, LLC
NDC code
71170-722-02
Origin
MO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0756-2026

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.

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