Carolina Infusion recalls TRI-MIX 50/2.5/25 Injectable vials due to lack of sterility assurance. Affected lots were manufactured with a specific batch number and expiration date. Consumers should check their vials for the lot number and expiration date.
Lack of Assurance of Sterility
Carolina Infusion is recalling TRI-MIX 50/2.5/25 Injectable vials because they may not be sterile. Using these vials could lead to infections if the product is not properly sterilized.
The vials may not be sterile, which can lead to infections if the product is used without proper sterilization. This is a serious risk for medical use, especially when administered via injection.
People who have received the TRI-MIX 50/2.5/25 Injectable vials from Carolina Infusion. Those using the product for medical purposes are most at risk due to potential infection.
Check the vial for the lot number 07052022@2 and expiration date 09/03/2022. The product is a prescription-only injectable medication.
Look for the lot number 07052022@2 and expiration date 09/03/2022 on the vial.
The recall indicates a lack of sterility assurance, so it is not safe to use without checking the recall details.
The recall does not specify a remedy, so contact Carolina Infusion for further instructions.
Check for the lot number 07052022@2 and expiration date 09/03/2022 on the vial.
We’ve drafted a message you can send Carolina Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-1532-2022 — Carolina Infusion Carolina Infusion Hello, I own a Carolina Infusion that is covered by recall D-1532-2022 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.
