Central Admixture Pharmacy Services recalls neonatal TPN starter bags with amino acids and calcium due to lack of sterility assurance. Affected units have specific NDC and lot numbers. Contact for remedy details.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services recalls neonatal TPN starter bags that may not be sterile. This could lead to infections in newborns receiving intravenous treatments.
The bags lack validation data for decontamination cycles, meaning they might not be sterile. If used without proper sterility, they could cause infections in newborns.
Newborns receiving intravenous treatments at hospitals using these specific neonatal TPN starter bags. Healthcare providers handling the recalled bags are at risk.
Check for NDC number 72196-0419-1 and lot numbers 36-251207 (expiring 7/10/2023) or 36-256337 (expiring 7/29/2023). These bags are for neonatal intravenous use only.
Look for NDC 72196-0419-1 and lot numbers 36-251207 or 36-256337 on the bag.
The recall is due to lack of validation data for decontamination cycles, which may mean the bags are not sterile.
The official notice does not specify a remedy, so contact Central Admixture Pharmacy Services for instructions.
Yes, lot numbers 36-251207 (expiring 7/10/2023) and 36-256337 (expiring 7/29/2023) are affected.
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-1004-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1004-2023 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.
