D-0750-2026 Class II Ongoing

Recalled by Apollo Care, LLC — Columbia, MO

FDA drug recall D-0750-2026 was initiated by Apollo Care, LLC on July 29, 2026 and is designated Class II. Reason for recall: Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material The recall status is ongoing. Affected quantity: 9,762 vials..

Recall Details

Product Type
Drugs
Report Date
August 19, 2026
Initiation Date
July 29, 2026
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
9,762 vials.

Product Description

SEMAGLUTIDE 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-812-03

Reason for Recall

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

Distribution Pattern

Nationwide within the U.S

Code Information

Lot: AC-017124, Exp. 8/30/2026; AC-017136, Exp. 12/31/2026.