Central Admixture Pharmacy Services recalls vancomycin dextrose solutions due to potential contamination. Products may not be sterile, posing infection risks. Check NDC 71285-6073-1 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 vancomycin dextrose solutions that may not be sterile. This could lead to infections if used in medical treatments. Patients and healthcare providers should check their product details to see if they are affected.
The FDA found potential contamination in the products intended to be sterile. This lack of sterility could cause infections during medical procedures if the solution is not properly sterilized.
Healthcare providers and patients using these vancomycin solutions for medical treatments. Those with the specific lot numbers and expiration dates listed are most at risk.
Check for the NDC code 71285-6073-1 and lot numbers 37-883198 through 37-892884 with expiration dates listed. These products are for prescription use only in central pharmacy settings.
Identify the NDC code 71285-6073-1 and lot numbers listed in the recall notice to determine if your product is affected.
The FDA has raised concerns about sterility, so these products may not be safe for medical use. Do not use until you confirm they are not affected.
Check the NDC code 71285-6073-1 and lot numbers listed in the recall notice for affected items.
Contact Central Admixture Pharmacy Services at 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106 for assistance with the recall.
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-0719-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0719-2023 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.
