Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Pyxis(TM) Anesthesia Station 4000 Recalled by CareFusion 303, Inc. Due to Potential fluid ingress of anesthesia station or med...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact CareFusion 303, Inc. directly.
Affected Products
BD Pyxis(TM) Anesthesia Station 4000, REF: 338
Quantity: 11,875 units
Why Was This Recalled?
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About CareFusion 303, Inc.
CareFusion 303, Inc. has 163 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report