Recall Z-1931-2024— CareFusion 303, Inc.
Class II · Ongoing
Class II FDA medical device recall by CareFusion 303, Inc., initiated 2024-04-15. FDA's recall record names no specific 510(k) clearance for this event. Product: BD Pyxis" Anesthesia Station ES, REF: 327. Reason: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire..
- Recalling firm
- CareFusion 303, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-04-15
- Firm location
- San Diego, CA, United States
Product description
BD Pyxis" Anesthesia Station ES, REF: 327
Reason for recall
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Data sourced from openFDA. This site is unofficial and independent of the FDA.