FDA recall record

Apollo Care SEMAGLUTIDE 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial recall — FDA D-0750-2026

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

Class IIclassification
D-0750-2026official record ID
Aug 19, 2026report date

Recall record at a glance

Official recordD-0750-2026
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmApollo Care, LLC
Report dateAug 19, 2026
Recall initiation dateJul 29, 2026
Quantity9,762 vials.
LocationColumbia, MO, United States

Official 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

Why the product was recalled

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

Distribution information

Nationwide within the U.S

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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