BD Pyxis Pro MedStation (CareFusion) – fluid ingress risk (2025)
This product may present a fire, explosion, or electrical hazard.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BD Pyxis Pro MedStation Main, REF: 1155-00
Brand
CareFusion 303, Inc.
Lot Codes / Batch Numbers
All Serial Numbers/Ref #/UDI: 1155-00 10885403521300
Products Sold
All Serial Numbers/Ref #/UDI: 1155-00 10885403521300
CareFusion 303, Inc. is recalling BD Pyxis Pro MedStation Main, REF: 1155-00 due to Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Recommended Action
Per FDA guidance
On September 30, 2025, BD issue a Urgent Medical Device Recall Expansion notification to affected consignees via FedEx. BD is asking consignees to take the following actions: 1. Affected products can continue to be used per existing Manuals and Guides. 2. In the event of an accidental fluid spill on the device or in a drawer, users should following instructions outlined within the customer notification. 3. Review the customer letter attachment which provides warnings, cautions and recommendations regarding fluid ingress. 4. Complete the attached Customer Response Form and return to the BD contact noted on the form whether or not you have any of the impacted material.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026