CareFusion 303, Inc. 2024-06-05 Health serious FDA
Health · FDA · Recall #FDA-Z-1932-2024
BD Pyxis(TM) Anesthesia Station 4000, REF: 338 Recall
Issued June 5, 2024 · CareFusion 303, Inc.
In June 2024, CareFusion 303, Inc. recalled the BD Pyxis(TM) Anesthesia Station 4000, REF: 338, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
What you should do
- 1 Stop using BD Pyxis(TM) Anesthesia Station 4000, REF: 338 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact CareFusion 303, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- CareFusion 303, Inc.
- Category
- Health
- Recall date
- June 5, 2024
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, K
- Recall number
- FDA-Z-1932-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- CareFusion 303, Inc. has 13 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.