Carolina Infusion recalls Semaglutide/Cyanocobalamin 24/2 MG/ML Injectable due to lack of sterility assurance. Affected lots were manufactured with specific dates and batch numbers.
Lack of Assurance of Sterility
Carolina Infusion is recalling Semaglutide/Cyanocobalamin 24/2 MG/ML Injectable products because they may not be sterile. This could lead to infections if the medication is used.
The product lacks assurance of sterility, meaning it could contain harmful bacteria or other contaminants. If the medication is injected, this could cause serious infections or other health issues.
People who have been prescribed this medication by a doctor and received the recalled product. Those using the medication for weight loss or diabetes management are at risk.
Check the product label for the lot number 08172022 and the expiration date of 09/16/2022. The product is a 0.4 ML syringe for prescription use.
Look for the lot number 08172022 and expiration date 09/16/2022 on the syringe packaging.
The recall states there is a lack of assurance of sterility, so it is not safe to use. The product may contain harmful contaminants.
The recall does not specify a remedy, so contact your doctor or pharmacist for guidance.
Check the product label for the lot number 08172022 and expiration date 09/16/2022.
We’ve drafted a message you can send Carolina Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-1521-2022 — Carolina Infusion Carolina Infusion Hello, I own a Carolina Infusion that is covered by recall D-1521-2022 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.
