Apollo Care recalls SEMAGLUTIDE 10mg vials due to particulate matter that could cause injection site reactions. Affected vials have NDC 71170-722-02 and lot AC-017274, expiring Dec 2026.
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Apollo Care is recalling SEMAGLUTIDE 10mg vials that may contain particulate matter. This could cause injection site reactions or other issues if used. The recall affects prescription-only vials sold in the U.S. with specific lot numbers.
Particulate matter (tiny fibers) in the vial could get into the injection site during use. This might cause irritation, inflammation, or other reactions at the injection site. The material is described as nylon/polyamide or silk/proteinaceous.
Prescription users of Apollo Care's SEMAGLUTIDE 10mg vials with NDC 71170-722-02 and lot AC-017274. People who have received this vial for weight management are most at risk.
Check for NDC 71170-722-02 and lot number AC-017274 on the vial label. The vial expires December 2026. This product is prescription-only for subcutaneous injection.
Look for NDC 71170-722-02 and lot AC-017274 on the vial label.
The recall states the vial may contain particulate matter that could cause injection site reactions. If you have this vial, you should check the label and contact your doctor.
The recall does not specify a remedy. Check the label for NDC 71170-722-02 and lot AC-017274, then contact your doctor for advice.
Look for NDC 71170-722-02 and lot AC-017274 on the vial label. The vial expires December 2026 and is prescription-only for subcutaneous injection.
We’ve drafted a message you can send Apollo Care to request your refund or repair — edit it as you like.
Subject: Recall D-0756-2026 — Apollo Care Apollo Care Hello, I own a Apollo Care that is covered by recall D-0756-2026 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.
