Carolina Infusion recalls specific TRI-MIX 30/1/20 injectable vials due to lack of sterility assurance. Affected vials have batch numbers listed in the recall notice. Consumers should check their vial lot numbers and contact the manufacturer for details.
Lack of Assurance of Sterility
Carolina Infusion is recalling certain TRI-MIX 30/1/20 injectable vials that may not be sterile. This could lead to infections if used improperly. Affected vials have specific batch numbers listed in the recall notice.
The vials may not be sterile, which could lead to infections if injected. This is a serious risk for medical use but the exact mechanism is not specified in the recall notice.
Patients prescribed this medication by a healthcare provider. Those using the vials without medical supervision are not affected.
Check the vial for batch numbers: 06272022, 07212022, 07292022, 08052022, 08102022, or 08122022. These vials were sold with specific expiration dates.
Look for batch numbers on the vial: 06272022, 07212022, 07292022, 08052022, 08102022, or 08122022.
The recall is due to a lack of assurance of sterility, which could lead to infections if used.
Check the vial batch number and contact Carolina Infusion if you have one of the affected batch numbers.
The recall states a lack of sterility assurance, which could cause infections, but the exact risk level is not specified in the notice.
We’ve drafted a message you can send Carolina Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-1527-2022 — Carolina Infusion Carolina Infusion Hello, I own a Carolina Infusion that is covered by recall D-1527-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
