Central Admixture Pharmacy Services recalls neonatal TPN starter bags with potential contamination. Products may not be sterile, posing risks to infants receiving treatment. 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 is recalling neonatal TPN starter bags that may not be sterile. This could harm infants receiving treatment through these bags, as the products are intended to be sterile but were found lacking in sterility during an FDA inspection.
The FDA found that the products intended to be sterile were not properly sterile. This means the bags could contain harmful bacteria or other contaminants that could cause infections in infants receiving treatment through these bags.
Parents or caregivers of infants receiving neonatal TPN treatment who use the recalled starter bags. Infants receiving treatment through these bags are at risk of infection.
Check for the product name 'Neonatal TPN Starter Bag, Amino Acids (Trophamine) 4%/Dextrose 10%' in 250 mL bags. Look for lot numbers 37-896130, 37-897957, 37-899605, or 37-901357 with expiration dates up to May 2023.
Identify the lot number and expiration date on the bag to confirm if it is recalled.
The FDA found that the products intended to be sterile were not properly sterile, which could lead to infections in infants receiving treatment.
Check the product details to confirm if it is recalled. If it is, contact Central Admixture Pharmacy Services for guidance.
Yes, the products may not be sterile, which could cause infections in infants receiving treatment.
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-0686-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0686-2023 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.
