Apollo Care recalls SEMAGLUTIDE 9mg vials due to particulate matter that could cause injection site reactions. Affected vials have specific NDC and lot numbers. Consumers should contact Apollo Care for details.
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Apollo Care is recalling SEMAGLUTIDE 9mg (4.5 mg/mL) vials that may contain particulate matter. This could lead to injection site reactions or other issues if used. The recall affects specific lot numbers and expiration dates.
The vials may contain small particles of nylon/polyamide and silk/proteinaceous material. These particles could cause irritation or reactions at the injection site when used.
People with prescriptions for SEMAGLUTIDE 9mg vials from Apollo Care. Those who have the specific lot numbers listed in the recall are most at risk.
Check for NDC 71170-822-02 with lot numbers AC-017125, AC-017138, AC-017147, AC-017214, AC-017226, or AC-017228. The vials expire by 8/30/2026 or 12/31/2026.
Look for NDC 71170-822-02 and specific lot numbers listed in the recall.
The vials may contain particulate matter, specifically nylon/polyamide and silk/proteinaceous material.
Contact Apollo Care directly for instructions on what to do with the vials.
Yes, the recalled vials have lot numbers AC-017125, AC-017138, AC-017147, AC-017214, AC-017226, or AC-017228.
We’ve drafted a message you can send Apollo Care to request your refund or repair — edit it as you like.
Subject: Recall D-0751-2026 — Apollo Care Apollo Care Hello, I own a Apollo Care that is covered by recall D-0751-2026 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.
