Central Admixture Pharmacy Services recalls phenylephrine IV bags (40mg/250ml) with NDC 72196-6092-1 that lack sterility assurance. Products may be contaminated and pose infection risks if used in medical procedures.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling phenylephrine IV bags that may not be sterile. Using these bags could lead to infections during medical procedures if the product is contaminated.
The bags lack validation data for decontamination cycles, meaning they may not be sterile. This could lead to infections if used in medical procedures without proper sterilization.
Healthcare professionals who prepare IV medications using these specific phenylephrine bags are affected. Patients receiving IV treatments with contaminated bags could face infection risks.
Check for the NDC number 72196-6092-1 on the bag. Products were manufactured with specific lot numbers between August 2023 and July 2024 and expire by various dates listed in the recall notice.
Look for the NDC number 72196-6092-1 and specific lot numbers listed in the recall notice.
The recall is due to lack of validation data for decontamination cycles, which means the bags may not be sterile.
The official recall notice does not specify a remedy or action for affected products.
Yes, the recall includes specific lot numbers from August 2023 to July 2024 with expiration dates listed in the notice.
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-0963-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0963-2023 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.
