Pyxis Pro MedStation units recalled over fluid ingress causing smoke or fire
CareFusion is recalling 27 BD Pyxis Pro MedStation Main units because potential fluid ingress of the anesthesia or med station may result in smoke, system downtime and/or fire.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Scored 3 under the risk-of-harm criterion: fluid ingress that may cause smoke or fire in a clinical dispensing unit is a hazard, and no injuries are reported.
Plain-English summary
The BD Pyxis Pro MedStation Main, REF 1155-00, is being recalled across all serial numbers.
Potential fluid ingress of the anesthesia station or med station may result in smoke, system downtime and/or fire.
The recall covers 27 units carrying UDI 10885403521300, distributed worldwide including nationwide in the United States and to Canada, the United Arab Emirates and Australia. The FDA has classified the action as Class II.
The enforcement record describes the failure mode and reports no injuries. Facilities operating affected units should follow the firm's instructions.
The recalled product
- Product
- BD Pyxis Pro MedStation Main, REF: 1155-00
- Manufacturer
- CareFusion 303, Inc.
- Affected units
- 27
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All Serial Numbers/Ref #/UDI: 1155-00 10885403521300
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 5 recalled by CareFusion 303, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 5 products in this recall →Related recalls
Same manufacturer · CareFusion 303, Inc.
See all →- HighBD Pyxis MedBank Mini fingerprint scanner may overheat and burn
FDA (Devices) · 2026-06-10
- HighBD Pyxis MedStation ES fingerprint scanner may overheat and burn
FDA (Devices) · 2026-06-10
- HighBD Pyxis Anesthesia Station fingerprint scanner may overheat and burn
FDA (Devices) · 2026-06-10
- HighBD Pyxis MedBank Tower fingerprint scanner may overheat and burn
FDA (Devices) · 2026-06-10
- HighBD Pyxis Mini Main cabinets may overheat at fingerprint scanner
FDA (Devices) · 2026-06-10
Same hazard · fluid ingress
See all →- HighMedication dispensing stations recalled over fluid ingress causing smoke or fire
FDA (Devices) · 2025-11-05
- HighPyxis Pro auxiliary drawers recalled over fluid ingress causing smoke or fire
FDA (Devices) · 2025-11-05
- HighPyxis Medbank units recalled over fluid ingress causing smoke or fire
FDA (Devices) · 2025-11-05
- HighControlled substance safe towers recalled over fluid ingress causing smoke or fire
FDA (Devices) · 2025-11-05
- HighStryker StrykeFlow suction irrigator may leak solution into the handpiece
FDA (Devices) · 2025-07-30