Central Admixture Pharmacy Services recalls EPINEPHrine dextrose 5% solutions due to potential contamination. Products may not be sterile, posing infection risks. Check NDC 71285-7018-1 and lot numbers for affected items.
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Central Admixture Pharmacy Services is recalling EPINEPHrine added to dextrose 5% solutions because an FDA inspection found possible contamination. This could lead to infections if used in medical settings.
The products were found to lack sterility assurance during an FDA inspection. This means the medication could be contaminated with bacteria, leading to infections if administered to patients.
Healthcare professionals and patients receiving this medication through central pharmacy services. Those using the product for medical treatments are most at risk.
Check for NDC 71285-7018-1 and lot numbers: 37-883218 (exp 04/30/2023), 37-885235 (exp 05/08/2023), and other listed lots. These products are for prescription use only in central pharmacy settings.
Verify the NDC code 71285-7018-1 and lot numbers listed in the recall notice to confirm if your product is affected.
No, the products were found to lack sterility assurance during an FDA inspection, so they should not be used.
Check the NDC code and lot numbers to see if your product is affected; if so, contact your healthcare provider for guidance.
The recall notice does not specify a replacement process; contact Central Admixture Pharmacy Services for assistance.
We’ve drafted a message you can send Central Admixture Pharmacy Services to request your refund or repair — edit it as you like.
Subject: Recall D-0729-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0729-2023 from Central Admixture Pharmacy Services. 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.
