Central Admixture Pharmacy Services recalls neonatal TPN starter bags due to unverified sanitization cycles. This may cause infections in infants receiving IV treatments. Affected units have specific NDC and lot numbers.
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling neonatal TPN starter bags that may not be sterile due to unvalidated sanitization cycles. This poses a risk of infection for infants receiving intravenous treatments.
The bags lack validated sanitization cycles, meaning they might not be sterile when used. This could lead to infections in infants who receive intravenous treatments through these bags.
Infants receiving intravenous treatments through these starter bags are at risk. Healthcare providers using the recalled product for neonatal care are most affected.
Check for NDC number 72196-0406-1 and lot numbers 36-262872 or 36-262873. The bags expire by August 27, 2023.
Verify the NDC number 72196-0406-1 and lot numbers 36-262872 or 36-262873 on the bag.
The recall states there is a lack of assurance of sterility due to unvalidated sanitization cycles, so it is not safe to use.
The recall does not specify a remedy, so contact the manufacturer for guidance.
Look for NDC number 72196-0406-1 and lot numbers 36-262872 or 36-262873 on the bag.
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-1116-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1116-2023 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.
