CareFusion recalls Pyxis MedStation ES and Anesthesia Station models with software issues that could cause wrong therapy doses, delays in dispensing, or unauthorized access. Affected units have specific catalog numbers and software versions.
Software issues could potentially result in: 1) delays in accessing dispensing software application, 2) wrong therapy (dose, item, timing, etc.), or 3) unauthorized access and/or compliance related issues
CareFusion is recalling Pyxis MedStation ES and Anesthesia Station devices due to software issues that might cause wrong therapy doses, delays in dispensing, or unauthorized access. This could affect medical staff using these devices for patient care.
Software issues in these devices could lead to incorrect therapy doses, delays in accessing dispensing software, or unauthorized access to system settings. These problems might occur during normal use when the device is operating.
Healthcare providers using Pyxis MedStation ES or Anesthesia Station devices for patient care are most at risk. The recall affects medical facilities that use these specific models.
Check for Pyxis MedStation ES (Catalog No. 323), Pyxis Anesthesia Station (PAS) (Catalog No. 327), or Pyxis MedStation ES Tower (Catalog No. 352). Also look for software versions v1.10 or earlier. The device may have a unique identifier (UDI-DI) listed in the recall details.
Verify the software version on your device; affected units have v1.10 or earlier.
Reach out to CareFusion directly for assistance with the recall process.
Software versions v1.10 and earlier are affected.
Check for Pyxis MedStation ES (Catalog No. 323), Pyxis Anesthesia Station (PAS) (Catalog No. 327), or Pyxis MedStation ES Tower (Catalog No. 352) with software version v1.10 or earlier.
No immediate stop is required; the recall involves software updates, not a safety hazard that requires immediate action.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-1119-2025 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-1119-2025 from CareFusion. 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.
