Apollo Care recalls SEMAGLUTIDE 12.5MG vials due to nylon/polyamide and 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 12.5mg semaglutide vials that may contain nylon or protein particles. Using these vials could cause injection site reactions or other issues.
The vials may contain small particles of nylon or protein. These particles could cause irritation or reactions at the injection site when used for subcutaneous injections.
People who have received a prescription for Apollo Care's 12.5mg semaglutide vials with the specified lot numbers and expiration dates are affected. Those using the product for weight management are most at risk.
Check the vial label for the product name 'SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial'. Look for lot numbers AC-017108 through AC-017225 with expiration dates up to 12/31/2026.
Look for the product name and lot numbers listed in the recall notice to confirm if your vial is affected.
The recall states the vials may contain particles that could cause injection site reactions, so it is not recommended to use these vials.
The recall does not specify a remedy, so you should check with your healthcare provider for guidance on safe alternatives.
Check the vial label for the lot numbers AC-017108 through AC-017225 with expiration dates up to 12/31/2026.
We’ve drafted a message you can send Apollo Care to request your refund or repair — edit it as you like.
Subject: Recall D-0747-2026 — Apollo Care Apollo Care Hello, I own a Apollo Care that is covered by recall D-0747-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
