Vital Care Compounder recalls SEMAGLUTIDE injections due to lack of sterility assurance. Products may contain contaminants that could cause infection. Affected lots and expiration dates provided.
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Vital Care Compounder is recalling SEMAGLUTIDE injections because FDA inspections found the products were not produced with enough sterility assurance. This means the injections could be contaminated, posing a risk of infection for users.
FDA inspections found the injections were produced without sufficient sterility assurance. This means the product could contain contaminants that might cause infections if injected.
People who have received the recalled SEMAGLUTIDE injections for weight management. Those using the product under a prescription are most at risk.
Check the lot numbers on the vial: 65680, 66043, 66372, or 66597. Products were sold with expiration dates from October 11, 2022, to October 29, 2022.
Look for lot numbers 65680, 66043, 66372, or 66597 on the vial.
FDA inspections found the product was not produced with enough sterility assurance, meaning it could contain contaminants that cause infections.
The recall record does not specify a remedy, so check the lot number and contact your healthcare provider for guidance.
Check the lot number on the vial: 65680, 66043, 66372, or 66597. Products were sold with expiration dates from October 11, 2022, to October 29, 2022.
We’ve drafted a message you can send Vital Care Compounder to request your refund or repair — edit it as you like.
Subject: Recall D-0053-2023 — Vital Care Compounder Vital Care Compounder Hello, I own a Vital Care Compounder that is covered by recall D-0053-2023 from Vital Care Compounder. 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.
