Carolina Infusion recalls L-Carnitine 500 mg/mL injectable vials due to lack of sterility assurance. This medication is prescription-only and may pose contamination risks if used.
Lack of Assurance of Sterility
Carolina Infusion is recalling L-Carnitine 500 mg/mL injectable vials because they lack assurance of sterility. This could lead to infections if the medication is used improperly.
The vials do not have proper sterility assurance, meaning they could be contaminated with bacteria or other pathogens. If injected, this could cause serious infections or health complications.
Prescription patients who have received the recalled L-Carnitine 500 mg/mL injectable vials. Healthcare providers using these vials for medical treatments are at risk.
Check for vials labeled 'L-Carnitine 500 mg/mL Injectable, 10 ML' with lot number 06132022@17 and expiration date 02/15/2023. The product is prescription-only and sold by Carolina Infusion.
Look for the lot number 06132022@17 and expiration date 02/15/2023 on the vial label.
The recall states there is a lack of assurance of sterility, so it is not safe to use as it could cause infections.
Check for vials labeled 'L-Carnitine 500 mg/mL Injectable, 10 ML' with lot number 06132022@17 and expiration date 02/15/2023.
The recall does not specify a remedy, so contact Carolina Infusion for guidance.
We’ve drafted a message you can send Carolina Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-1515-2022 — Carolina Infusion Carolina Infusion Hello, I own a Carolina Infusion that is covered by recall D-1515-2022 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.
