Central Admixture Pharmacy Services recalls specific lots of epinephrine dextrose 5% solutions because FDA found potential sterility issues. These products are for medical use only and must be discarded if recalled.
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 has recalled specific lots of epinephrine dextrose 5% solutions due to concerns about sterility after an FDA inspection. This means the products could be contaminated and unsafe for medical use.
The FDA inspection raised concerns that the products might not be sterile, which could lead to infections or other serious health issues if used in medical procedures. These solutions are intended for injection only and are critical for treating certain medical conditions.
Healthcare facilities and medical professionals who use these specific lots of epinephrine dextrose solutions for injections. Patients receiving these products through medical facilities are at risk.
Check the product label for the lot numbers: 37-884448 through 37-898559. The expiration dates range from May 4, 2023 to June 29, 2023. These products are for medical use only and are sold in 250 mL bags.
Discard any epinephrine dextrose 5% solutions with the listed lot numbers immediately.
The FDA found potential sterility issues in these products after an inspection, which could lead to infections if used.
Discard the product immediately if it has one of the listed lot numbers.
No, these specific lots are not safe due to potential contamination 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-0701-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0701-2023 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.
