Central Admixture Pharmacy Services recalls fentanyl 250mL bags due to lack of sterility validation. These are prescription-only drugs for medical use. No remedy specified in official notice.
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling fentanyl 250mL bags that may not be sterile. This poses a risk of infection or contamination for patients receiving these drugs through medical facilities.
The bags lack validated sanitization cycles, meaning they might not be sterile. This could lead to infections or contamination in medical settings where the drugs are administered.
Healthcare facilities using these fentanyl bags for medical treatments. Patients receiving injections through these bags are at risk of infection.
Check for the product name 'fentaNYL in 0.9% sodium chloride, 5000 mcg/250 mL' with NDC 71286-2074-1. Look for specific lot numbers listed in the recall notice.
Identify the NDC number 71286-2074-1 and lot numbers from the recall list.
The official recall states there is a lack of sterility assurance, so it is not safe for medical use.
Look for the NDC 71286-2074-1 and specific lot numbers listed in the recall notice.
The official notice does not specify a remedy, so contact the manufacturer for guidance.
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-1063-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1063-2023 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.