CareFusion recalls BD Pyxis Anesthesia Station ES models with specific software versions due to sync errors that could lead to incorrect medication dispensing. Affected units may need software updates to prevent safety issues.
Sync timeout may occur between the server and automated dispensing device, due to a server software error which may occur if syncing a large amount of data that takes excessive time, which may cause the dispensing devices to become disconnected from the ES server; dispensing devices will not receive updated information, which may lead to incorrect therapy, and delay in accessing medication.
CareFusion is recalling BD Pyxis Anesthesia Station ES models that have software versions prone to sync errors. This could cause dispensing devices to disconnect from the server, leading to incorrect medication administration or delays in accessing critical drugs.
The server software error can cause the dispensing devices to become disconnected from the ES server when syncing large amounts of data. This disconnect may result in the devices not receiving updated information, potentially leading to incorrect medication administration or delays in accessing critical drugs.
Healthcare facilities using BD Pyxis Anesthesia Station ES models with the listed software versions are most at risk. Patients receiving medication through these systems could be affected if the device disconnects from the server.
Check if your BD Pyxis Anesthesia Station ES model has the specific software versions listed: 1.7.4.128, 1.7.4.134, 1.7.4.136, 1.7.4.137, All 1.7.1, All 1.7.2, or All 1.7.3. The affected models include Anesthesia Station ES (REF: 327), MedStation ES (REF: 323), and others as detailed in the recall notice.
Verify your device's software version against the list of affected versions provided in the recall notice.
Affected software versions include 1.7.4.128, 1.7.4.134, 1.7.4.136, 1.7.4.137, All 1.7.1, All 1.7.2, and All 1.7.3.
Check if your BD Pyxis Anesthesia Station ES model has the specific software versions listed in the recall notice, such as Anesthesia Station ES (REF: 327) or MedStation ES (REF: 323).
The recall notice does not specify a remedy, so you should check the official CareFusion website for updates or contact their support for guidance.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-1375-2025 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-1375-2025 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.
