FDA · Drugs ·
SEMAGLUTIDE 10mg (5mg/mL) recall
Apollo Care, LLC recalled SEMAGLUTIDE 10mg (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 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
Quantity: 500 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 noticeDetails
- 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-0756-2026
- Source
- U.S. Food and Drug Administration
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