Central Admixture Pharmacy Services recalls phenylephrine 25mg IV bags with potential sterility issues. These bags may cause infections if used improperly. Check lot numbers and contact for details.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services has recalled phenylephrine 25mg IV bags due to insufficient sterility validation. Using these bags without proper sterilization could lead to infections in medical settings.
The bags lack validation data for decontamination cycles, meaning they might not be sterile. This could lead to infections if used in medical procedures without proper sterilization.
Healthcare professionals using these IV bags for medical treatments. Patients receiving IV therapy with the recalled bags are at risk of infection.
Check for lot numbers 36-249691, 36-249692, 36-250052, 36-250053, 36-251062, 36-251992, or 36-252467. The bags expire by August 2023.
Look for lot numbers 36-249691, 36-249692, 36-250052, 36-250053, 36-251062, 36-251992, or 36-252467 on the bag.
The bags lack validation data for decontamination cycles, which could lead to infections if not properly sterilized.
Check the lot numbers on the bag: 36-249691, 36-249692, 36-250052, 36-250053, 36-251062, 36-251992, or 36-252467.
The recall does not specify a remedy, so contact Central Admixture Pharmacy Services 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-0962-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0962-2023 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.
