Recalled BD Pyxis Medbank models with reference numbers 1137-00 to 155169-01 may experience fluid ingress leading to smoke, system downtime, or fire. Consumers should check their device serial numbers.
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
CareFusion recalls various BD Pyxis Medbank models due to a potential risk of fluid entering the anesthesia or med station, which could cause smoke, system shutdowns, or fire. This affects medical devices used in healthcare settings.
Fluid ingress into the anesthesia or med station can cause smoke, system downtime, or fire. This occurs when the device's internal components are exposed to fluids, potentially leading to malfunction or fire hazards.
Healthcare professionals and facilities using the recalled BD Pyxis Medbank models are most at risk. The device is used for medical infusion systems in hospitals and clinics.
Check your BD Pyxis Medbank device for reference numbers listed in the recall: 1137-00 through 155169-01. Serial numbers are provided in the recall list for specific models.
Look for the reference number on your BD Pyxis Medbank device. The recall includes models with reference numbers from 1137-00 to 155169-01.
The recall includes BD Pyxis Medbank models with reference numbers from 1137-00 to 155169-01.
The recall does not specify a remedy; the manufacturer has not provided a fix or replacement.
Check your device's reference number against the list of 1137-00 to 155169-01 provided in the recall notice.
We’ve drafted a message you can send BD Pyxis Medbank to request your refund or repair — edit it as you like.
Subject: Recall Z-0367-2026 — BD Pyxis Medbank BD Pyxis Medbank Hello, I own a BD Pyxis Medbank that is covered by recall Z-0367-2026 from BD Pyxis Medbank. 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.
