Carolina Infusion recalls specific TRI-MIX 30/2/20 10ml vials due to lack of sterility assurance. Affected vials have batch numbers listed in the recall notice.
Lack of Assurance of Sterility
Carolina Infusion is recalling certain TRI-MIX 30/2/20 10ml injectable vials because they may not be sterile. This could lead to infections if used improperly.
The vials may not be sterile, which could cause infections if injected. This is a serious risk for patients receiving the medication.
Patients prescribed this medication by a healthcare provider. Those using the product without medical supervision are not affected.
Check for batch numbers: 07052022@10, 07052022@16, 07122022@11, 07182022@17, 07202022@6, 07252022@9, 0729202222@2, 07292022@13, 08122022@9, 08162022@2, or 082620222@1. The vials are prescription-only.
Look for batch numbers listed in the recall notice: 07052022@10, 07052022@16, 07122022@11, 07182022@17, 07202022@6, 07252022@9, 0729202222@2, 07292022@13, 08122022@9, 08162022@2, or 082620222@1.
The recall states the vials may not be sterile, so they are not safe for injection without proper sterility assurance.
Check the batch number on the vial. The recalled batch numbers are listed in the recall notice.
The recall does not specify a remedy, so contact Carolina Infusion for further instructions.
We’ve drafted a message you can send Carolina Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-1530-2022 — Carolina Infusion Carolina Infusion Hello, I own a Carolina Infusion that is covered by recall D-1530-2022 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.
