Central Admixture Pharmacy Services recalls neonatal TPN starter bags with potential contamination. Products may not be sterile, posing infection risks for infants. Check lot numbers and contact for recalls.
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 neonatal TPN starter bags that may not be sterile, which could lead to infections in infants. Healthcare providers using these products should stop using the affected lots immediately.
The FDA found that the products intended to be sterile may not have been properly sterilized. This lack of sterility could lead to infections in infants who receive the products through intravenous feeding.
Healthcare providers administering neonatal TPN (total parenteral nutrition) to infants. Infants receiving treatment with these bags are at highest risk.
Check the lot numbers: 37-894338, 37-896505, 37-898301, 37-898305, or 37-900061. Products expire by April 29, 2023, May 7, 2023, May 14, 2023, or May 21, 2023.
Immediately stop using the recalled neonatal TPN starter bags with the listed lot numbers.
Neonatal TPN Starter Bag, Amino Acids (Trophamine) 3%/Dextrose 5% with low calcium and HEPARIN, packaged in 250 mL per bag.
Lot numbers 37-894338, 37-896505, 37-898301, 37-898305, and 37-900061.
Check the lot number on the product label; affected lots expire by April 29, 2023, May 7, 2023, May 14, 2023, or May 21, 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-0696-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0696-2023 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.
