Central Admixture Pharmacy Services recalls Plasma-Lyte A transplant solution due to potential contamination. Products may not be sterile, posing infection risks. Check NDC 71285-0014-2 and lot # 37-897801.
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 Plasma-Lyte A transplant solution bags that may not be sterile, risking infections. This affects medical use only, not general consumers.
The FDA found potential contamination in the sterile solution. If not properly sterile, the product could cause infections in patients during medical procedures.
Healthcare professionals using this product for medical treatments. Patients receiving transplants or critical care are at risk if the solution is contaminated.
Check for NDC 71285-0014-2 and lot number 37-897801 on the packaging. Products were sold by Central Admixture Pharmacy Services in Allentown, PA.
Look for NDC 71285-0014-2 and lot number 37-897801 on the packaging.
No, this is a prescription-only medical product for transplant patients. General consumers do not use this product.
The recall does not specify a remedy. Check with your healthcare provider for guidance.
Look for NDC 71285-0014-2 and lot number 37-897801 on the packaging. Products were sold by Central Admixture Pharmacy Services in Allentown, PA.
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-0657-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0657-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
