Carolina Infusion recalls 12.6mL TEST CYP/PROP injectable vials due to lack of sterility assurance. This could lead to infections if used improperly. Affected lots: 07052022.
Lack of Assurance of Sterility
Carolina Infusion is recalling 12.6 mL TEST CYP/PROP (50:50) 100 mg/100 mg/ml injectable vials because they lack sterility assurance. Using these vials could lead to infections if they are not properly sterilized before use.
The vials lack assurance of sterility, meaning they might not be clean enough to prevent infections when injected. This is a serious risk for patients receiving the medication through injection.
Prescription drug users who have the specific vial lot number 07052022 are affected. Healthcare providers and patients using this medication under a prescription are at risk.
Check for the lot number 07052022 on the vial label. The product is a 12.6 mL injectable vial with the name TEST CYP/PROP (50:50) 100 mg/100 mg/ml.
Look for the lot number 07052022 on the vial label to confirm if it is affected.
The recall states there is a lack of sterility assurance, so it is not safe to use without proper sterilization.
The recall does not specify a remedy, so contact Carolina Infusion for guidance.
Check the vial label for the lot number 07052022.
We’ve drafted a message you can send Carolina Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-1525-2022 — Carolina Infusion Carolina Infusion Hello, I own a Carolina Infusion that is covered by recall D-1525-2022 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.
