Carolina Infusion recalls Semaglutide/Cyanocobalamin 10/2 MG/ML Injectable due to lack of sterility assurance. Affected lots: 08152022@14, batch date 09/14/2022.
Lack of Assurance of Sterility
Carolina Infusion is recalling Semaglutide/Cyanocobalamin 10/2 MG/ML Injectable products because they may not be sterile. This could lead to infections if used improperly.
The product lacks assurance of sterility, meaning it might contain harmful bacteria or other contaminants. If injected, this could cause serious infections or other health issues.
People who have received the recalled Semaglutide/Cyanocobalamin 10/2 MG/ML Injectable product from Carolina Infusion. Those with medical conditions requiring injections are at higher risk.
Check for the lot number 08152022@14 on the product label. The product was manufactured with a batch date of 09/14/2022 and sold by Carolina Infusion LLC.
Look for the lot number 08152022@14 on the syringe label.
The recall states there is a lack of assurance of sterility, so it may not be safe. Do not use the product until you confirm it's not recalled.
The recall does not specify a remedy, so contact Carolina Infusion for guidance on next steps.
Check for the lot number 08152022@14 on the product label. The product was manufactured with a batch date of 09/14/2022.
We’ve drafted a message you can send Carolina Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-1520-2022 — Carolina Infusion Carolina Infusion Hello, I own a Carolina Infusion that is covered by recall D-1520-2022 from Carolina Infusion. 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.
