Central Admixture Pharmacy Services recalls neonatal TPN starter bags with potential sterility issues. Products may not be sterile, risking infection in infants. Stop using immediately if you have these bags.
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 found to lack sterility assurance by the FDA during an inspection. This means the bags could contain harmful bacteria, leading to serious infections in infants who receive the treatment.
Infants receiving neonatal TPN treatment using these specific starter bags. Healthcare providers and parents who administer the treatment are most at risk.
Check for the product name: Neonatal TPN Starter Bag, Amino Acids (Trophamine) 6%/Dextrose 10% with CALCIUM and HEPARIN. Look for lot numbers 37-896152, 37-897923, or 37-899173 with expiration dates up to May 2023.
Discard the recalled neonatal TPN starter bags if you have them.
The FDA found that the products lacked sterility assurance during an inspection, which could lead to infections in infants.
Discard the recalled bags immediately and contact your healthcare provider for alternative treatment options.
Yes, check for lot numbers 37-896152, 37-897923, or 37-899173 with expiration dates up to May 2023.
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-0694-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0694-2023 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.
