Apollo Care recalls 0.9mg SEMAGLUTIDE vials due to nylon/polyamide and silk/proteinaceous particulate matter that could cause injection site reactions.
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Apollo Care is recalling 0.9mg SEMAGLUTIDE vials that may contain particulate matter. This could cause injection site reactions or other adverse effects if used.
The vials may contain small particles of nylon/polyamide and silk/proteinaceous material. These particles could enter the bloodstream during injection, potentially causing injection site reactions or other adverse effects.
People with prescriptions for Apollo Care's SEMAGLUTIDE 0.9mg vials. Those who have received the vial with lot number AC-017131 are most at risk.
Check for the vial labeled 'SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only'. Look for lot number AC-017131 on the vial.
Look for the lot number AC-017131 on the vial to confirm if it is recalled.
The recall does not state that the product is safe to use; it may contain particulate matter that could cause injection site reactions.
The recall record does not specify a remedy, so no action is required beyond checking the lot number.
Check for the lot number AC-017131 on the vial label.
We’ve drafted a message you can send Apollo Care to request your refund or repair — edit it as you like.
Subject: Recall D-0752-2026 — Apollo Care Apollo Care Hello, I own a Apollo Care that is covered by recall D-0752-2026 from Apollo Care. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
