Central Admixture Pharmacy Services recalls neonatal TPN starter bags with potential sterility issues. Products may not be sterile, risking infection in infants. Check lot numbers and 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 lead to infections in infants receiving the treatment. The recall is due to FDA concerns about sterility after an inspection.
The products were inspected by the FDA and found to lack assurance of sterility. This means the bags could contain harmful bacteria, potentially causing infections in infants who receive the treatment.
Infants receiving neonatal TPN treatment via these starter bags. Healthcare providers using the products are most at risk.
Check for lot numbers: 37-893819 to 37-900058. Products expire by April 2023 to May 2023. These are neonatal TPN starter bags with amino acids and dextrose.
Look for lot numbers on the bag: 37-893819 through 37-900058.
Reach out to Central Admixture Pharmacy Services for further assistance or to confirm if your product is affected.
The FDA found that the products lacked assurance of sterility after an inspection, which could lead to infections in infants.
Check the lot number on the bag. If it matches the listed numbers, contact Central Admixture Pharmacy Services for guidance.
Yes, the products may not be sterile, which could cause infections in infants receiving the 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-0693-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0693-2023 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.
