Central Admixture Pharmacy Services recalls neonatal TPN starter bags with potential lack of sterility. This could cause infection in infants receiving IV treatment. Affected units have specific NDC and lot numbers.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling neonatal TPN starter bags that may not be sterile. This poses a risk of infection for infants receiving intravenous treatment. The recall affects specific batch numbers with a known expiration date.
The product lacks validation data for decontamination cycles, meaning it may not be sterile. This could lead to infections in infants who receive the treatment through this bag. The risk is specific to the product's intended use in neonatal care.
Infants receiving intravenous treatment with this specific TPN starter bag are at risk. Healthcare providers using the recalled product for neonatal care may need to switch to alternatives.
Check for the NDC number 72196-0407-1 and lot number 36-251206 on the bag. The product expires July 10, 2023, and is only for prescription use in neonatal care.
Look for NDC 72196-0407-1 and lot number 36-251206 on the bag.
The recall states there is a lack of assurance of sterility, so it is not safe for use in neonatal care.
The recall does not specify a remedy, so contact the manufacturer for guidance.
The product was manufactured with lot number 36-251206, expiring July 10, 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-1007-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1007-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
