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FDAFDA · Food and drugs·Recall number Z-0370-2026

BD Pyxis Pro MedStation Main, REF: 1155-00

Published November 5, 2025 · Recall initiated: September 30, 2025

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
CareFusion 303, Inc.
Distributor
Worldwide distribution - US Nationwide and the countries of Canada, United Arab Emirates, Australia.
Lot
All Serial Numbers/Ref #/UDI: 1155-00 10885403521300
Risk classification
Class II
Area (FDA)
device
Country
United States

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