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FDA · Drugs ·

SEMAGLUTIDE 12.5MG (2.5MG/mL) recall

Apollo Care, LLC recalled SEMAGLUTIDE 12.5MG (2.5MG/mL) on August 19, 2026 because of presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material. It was sold nationwide.

Why it was recalled

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

What's recalled

SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-495-05

Quantity: 56,918 vials.

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Apollo Care, LLC, Columbia, MO
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
Nationwide within the U.S
Status
Ongoing
Recall number
D-0747-2026
Source
U.S. Food and Drug Administration

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