Recall of BD Pyxis ES Enterprise Server devices with specific catalog numbers and software versions due to potential failure to receive timely patient and medication updates from enterprise systems.
Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems.
CareFusion recalls BD Pyxis ES Enterprise Server devices that may not receive timely updates of patient or medication information from connected systems. This could lead to errors in medication administration if the system fails to communicate properly with enterprise systems.
The software issue may prevent the device from receiving critical updates from enterprise systems, potentially causing medication administration errors. This could happen if the system does not communicate properly with other hospital systems that manage patient information and medication orders.
Healthcare facilities using BD Pyxis ES Enterprise Server devices with catalog numbers listed in the recall. Staff responsible for medication administration are most at risk if the system fails to update patient information.
Check if your BD Pyxis ES Enterprise Server has catalog numbers listed in the recall (e.g., 1115-00, 137672-02) and software versions 1.6.1 to 1.11.0 with server applications ES 4.13 to 5.8.X.
Identify your BD Pyxis ES Enterprise Server's catalog number from the list provided in the recall notice.
Confirm your device's software version is within the range 1.6.1 to 1.11.0 with server applications ES 4.13 to 5.8.X.
The recall states a software issue may result in the device not receiving timely updates of patient, medication, or related information from enterprise systems.
No, the recall does not require immediate stop use. The hazard is described as a potential communication issue, not an immediate safety risk.
Check your device's catalog number against the list provided in the recall and verify your software version is within the range 1.6.1 to 1.11.0 with server applications ES 4.13 to 5.8.X.
We’ve drafted a message you can send BD to request your refund or repair — edit it as you like.
Subject: Recall Z-1028-2026 — BD BD Hello, I own a BD that is covered by recall Z-1028-2026 from BD. 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.
