FDA·Medicines·August 19, 2026

Apollo Care recalls semaglutide multi-dose vials over particles found in the product

The vials contain particulate matter, which the notice identifies as a nylon/polyamide and silk/proteinaceous-type material.

What to do

The notice does not give instructions. Read the official notice for details.

Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.

Recall details

Product
SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-721-01; 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; SEMAGLUTIDE…
Hazard
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Units
250 vials.; 56,918 vials.; 23,029 vials.
Where sold
Nationwide within the U.S
FDA classification
Class II · Ongoing
Classified by FDA
August 7, 2026
Recall started
July 29, 2026
FDA enforcement report
August 19, 2026
Identifiers
  • Codes: Lot: AC-017273, Exp. 12/12/2026.
  • FDA recall number: D-0755-2026
  • Codes: Lot: AC-017108, Exp. 11/17/2026; AC-017110, Exp. 11/20/2026; AC-017112, Exp. 11/21/2026; AC-017142, AC-017144, Exp. 12/10/2026; AC-017166, AC-017167, AC-017177, AC-017213, AC-017224, AC-017225, Exp. 12/31/2026
  • FDA recall number: D-0747-2026
  • Codes: Lot: AC-017114, Exp. 11/24/2026; AC-017164, AC-017204, AC-017205, Exp. 12/31/2026.
  • FDA recall number: D-0748-2026
  • Codes: Lot: AC-017271, Exp. 12/12/2026.
  • FDA recall number: D-0753-2026
  • Codes: Lot: C-017115, Exp. 11/25/2026; AC-017163, Exp. 12/31/2026; AC-017169, AC-017170, AC-017171, Exp. 12/31/2026; AC-017230, AC-017231, Exp. 5/5/2027.
  • FDA recall number: D-0749-2026
  • Codes: Lot: AC-017131, Exp. 8/30/2026.
  • FDA recall number: D-0752-2026

The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.

Official notice

The notice's own wording from FDA.

Product
SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-721-01 | 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 | 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 | SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-711-02
Reason for recall
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Classification
Class II (Ongoing)
Distribution
Nationwide within the U.S
Quantity
250 vials.; 56,918 vials.; 23,029 vials.; 37,546 vials.; 4,748 vials.; 4,250 vials.

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