Carolina Infusion recalls TEST CYP/DHEA (Sesame) 200 MG/2.5 MG/ML Injectable vials due to lack of sterility assurance. Affected lots from 06012022 to 08232022 with expiration dates through November 2022.
Lack of Assurance of Sterility
Carolina Infusion is recalling specific lots of TEST CYP/DHEA (Sesame) 200 MG/2.5 MG/ML Injectable vials because they lack sterility assurance. Using these vials could lead to infections or other health risks if the product is not properly sterilized.
The vials lack proper sterility assurance, meaning they could be contaminated with bacteria or other pathogens. This contamination could lead to infections or other health issues if the product is used without proper sterilization.
People who purchased or have the TEST CYP/DHEA (Sesame) 200 MG/2.5 MG/ML Injectable vials from Carolina Infusion between June 2022 and August 2022. Those using these vials for medical purposes are at risk of infection due to potential contamination.
Check for vials labeled 'TEST CYP/DHEA (Sesame) 200 MG/2.5 MG/ML Injectable, 10 ML' with lot numbers from 06012022 to 08232022. The expiration dates range from August 30, 2022, to November 2022.
Look for lot numbers on the vial between 06012022 and 08232022.
If the vial has a lot number in the affected range, discard it immediately to avoid potential infection.
TEST CYP/DHEA (Sesame) 200 MG/2.5 MG/ML Injectable, 10 ML vial.
Lots from 06012022 to 08232022 with expiration dates through November 2022.
Check the vial for lot numbers between 06012022 and 08232022. The product was sold by Carolina Infusion between June and August 2022.
We’ve drafted a message you can send Carolina Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-1524-2022 — Carolina Infusion Carolina Infusion Hello, I own a Carolina Infusion that is covered by recall D-1524-2022 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.
