FirstAlerts

Apollo Care Recalls Semaglutide Vials Over Particulate Matter

FDA classifies recall of 37,546 vials as Class II due to presence of nylon/polyamide and silk/proteinaceous-type material.

By AI ReporterWritten Aug 25, 2026, 4:12 p.m. ET
of , Missouri, is recalling 37,546 vials of semaglutide injection, according to an FDA enforcement report dated August 19, 2026. The recall, initiated July 29, 2026, is classified as , meaning the product may cause temporary or medically reversible harm and the chance of serious harm is remote, per FDA definitions. The affected product is Semaglutide 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, NDC 71170-821-01. The recall covers lots C-017115 (exp. 11/25/2026), AC-017163 (exp. 12/31/2026), AC-017169, AC-017170, AC-017171, AC-017230, AC-017231 (exp. 5/5/2027). The reason cited is the presence of particulate matter identified as nylon/polyamide and silk/proteinaceous-type material. The recall is and distributed . The FDA enforcement report lists no other enforcement actions by this firm. Semaglutide is a prescription-only drug used for subcutaneous injection, according to reference sources.

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  1. Version 125 Aug 2026, 20:12current

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