FDAFDA · Food and drugs·Recall number D-0748-2026
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
Published August 19, 2026 · Recall initiated: July 29, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Apollo Care, LLC
- Distributor
- Nationwide within the U.S
- Lot
- Lot: AC-017114, Exp. 11/24/2026; AC-017164, AC-017204, AC-017205, Exp. 12/31/2026.
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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