CareFusion recalls BD Pyxis Pro 7-Drawer Auxiliary models with reference numbers 1149-00 and 1152-00 due to potential fluid ingress causing smoke, system downtime, or fire.
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
CareFusion is recalling specific models of BD Pyxis Pro 7-Drawer Auxiliary medical devices because fluid can enter the system, potentially causing smoke, system shutdowns, or fire. This risk affects healthcare facilities using these devices for anesthesia or medication delivery.
Fluid ingress into the anesthesia or med station can cause smoke, system shutdowns, or fire. This happens when the device's internal components are exposed to moisture or other fluids, which may occur during normal use in medical settings.
Healthcare facilities that own or use the recalled BD Pyxis Pro 7-Drawer Auxiliary models are most at risk, particularly those handling anesthesia or medications where system reliability is critical.
Check for reference numbers 1149-00 or 1152-00 on the device. The specific serial numbers 10885403517822 and 10885403517839 are also affected.
Verify the reference number on the device to confirm if it matches 1149-00 or 1152-00.
Reach out to CareFusion for guidance on next steps if the device is affected.
The affected models are BD Pyxis Pro 7-Drawer Auxiliary with reference numbers 1149-00 and 1152-00, including serial numbers 10885403517822 and 10885403517839.
The recall record does not specify a remedy, so no immediate fix is provided.
Check for reference numbers 1149-00 or 1152-00 on the device, or serial numbers 10885403517822 and 10885403517839.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0369-2026 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-0369-2026 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.
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.
