Carolina Infusion recalls QUAD-MIX 30/2/60/0.15 Injectable vials due to lack of sterility assurance. This could lead to infections if used improperly. Check lot numbers for affected products.
Lack of Assurance of Sterility
Carolina Infusion is recalling QUAD-MIX 30/2/60/0.15 Injectable vials because they may not be sterile. Using these vials could cause infections, especially in medical treatments.
The vials may not be sterile, which can lead to infections if the medication is injected. This risk is particularly concerning for medical treatments where sterility is critical.
Patients prescribed this medication by a healthcare provider. Those using the product without medical supervision are not affected.
Check for vials labeled QUAD-MIX 30/2/60/0.15 Injectable, 5 ML, Rx only. Lot number 08022022@12 was produced on 2022-02-08 with a use-by date of 2022-10-01.
Look for the lot number 08022022@12 on the vial label to confirm if it's affected.
The recall states there is a lack of assurance of sterility, so it is not safe to use without checking the lot number.
The recall does not specify a remedy, so contact Carolina Infusion for guidance on next steps.
Check for vials labeled QUAD-MIX 30/2/60/0.15 Injectable, 5 ML, Rx only with lot number 08022022@12.
We’ve drafted a message you can send Carolina Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-1533-2022 — Carolina Infusion Carolina Infusion Hello, I own a Carolina Infusion that is covered by recall D-1533-2022 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.
