BD Pyxis MedStations and Medbanks Recalled for Fire and Smoke Risk

Summary

CareFusion 303, Inc. (part of BD) has recalled 11,519 BD Pyxis medication and anesthesia management systems, including Medbank, MedFlex, and Pro MedStation models. The recall was issued because liquids can leak into the devices, potentially causing an electrical short that leads to system failure, smoke, or an active fire. While no specific injuries are mentioned in this notice, the manufacturer has identified a safety hazard that could cause device downtime or pose a risk of fire in medical facilities. These stations were distributed nationwide and internationally between various manufacturing dates.

Risk

The internal components of the medication stations are susceptible to fluid ingress, where liquid enters the electronics. If liquid comes into contact with the station's power or control boards, it can cause electrical arcing, resulting in smoke production or a fire. This defect can lead to system shutdowns that delay medication delivery or pose a direct burn and smoke inhalation risk to patients and healthcare staff.

Additional Information