Apollo Care recalls SEMAGLUTIDE 5mg vials due to potential particulate matter that could cause injection site reactions. Affected vials have specific NDC and lot numbers.
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Apollo Care is recalling SEMAGLUTIDE 5mg (1mg/mL) vials that may contain particulate matter. This could lead to injection site reactions or other issues if used as intended.
The vials may contain small particles of nylon/polyamide and silk/protein materials. These particles could enter the bloodstream during injection, potentially causing irritation or reactions at the injection site.
People with prescriptions for this medication who received vials with NDC 71170-712-03 and lot number AC-017272. Those using the product for weight management are most at risk.
Check for the NDC number 71170-712-03 and lot number AC-017272 on the vial label. The product was sold by Apollo Care in Columbia, Missouri, with an expiration date of December 2026.
Look for the NDC number 71170-712-03 and lot number AC-017272 on the vial label.
The recall is due to potential particulate matter that could cause injection site reactions. The product may still be safe if the vial is checked for the specific lot number and NDC.
The recall does not specify a remedy, so check the vial label for the NDC number 71170-712-03 and lot number AC-017272. If it matches, contact Apollo Care for further instructions.
Check the vial label for the NDC number 71170-712-03 and lot number AC-017272. The product was sold by Apollo Care in Columbia, Missouri, with an expiration date of December 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-0754-2026 — Apollo Care Apollo Care Hello, I own a Apollo Care that is covered by recall D-0754-2026 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.
