Central Admixture Pharmacy Services recalls EPINEPHrine dextrose 5% products due to potential sterility issues found during FDA inspection. Discard or contact for details.
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 recalls specific EPINEPHrine dextrose 5% products because an FDA inspection raised concerns about their sterility. Using these products could lead to infections if they are not sterile.
The FDA inspection found potential sterility issues in the products. This means the products might not be sterile when they should be, which could cause infections if used in medical procedures.
Healthcare professionals using these products in hospitals or clinics. Patients receiving these medications through intravenous administration are at risk if the products are not sterile.
Check for the lot numbers: 37-884156 to 37-900073. These products were sold with expiration dates from May 2023 through June 2023. They are labeled as 'EPINEPHrine added to dextrose 5%, 8 mg/250 mL' for prescription use.
Look for lot numbers on the product label: 37-884156 through 37-900073.
If you have the recalled products, discard them immediately to avoid potential infection risks.
An FDA inspection raised concerns about the sterility of these products, which could lead to infections if used improperly.
Check the product label for lot numbers 37-884156 to 37-900073, which were produced between May and June 2023.
Discard the product immediately to avoid potential infection risks.
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-0730-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0730-2023 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.
