CareFusion 303, Inc. 2024-03-13 Health serious FDA
Health · FDA · Recall #FDA-Z-1223-2024
BD Pyxis: MedStation ES, REF: 323; Anesthesia Station ES, REF: 327; MedStation ES Tower,… Recall
Issued March 13, 2024 · CareFusion 303, Inc.
In March 2024, CareFusion 303, Inc. recalled the BD Pyxis: MedStation ES, REF: 323; Anesthesia Station ES, REF: 327; MedStation ES Tower,…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Automated dispensing cabinets, running affected software, and Windows 10 operating system may experience the application randomly hang, freeze and/or crash, which may result in delays in medication access, and potential data loss.
What you should do
- 1 Stop using BD Pyxis: MedStation ES, REF: 323; Anesthesia Station ES, REF: 327; MedStation ES Tower,… 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
- March 13, 2024
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide distribution including in the states of VA, SC, IL, AL, KS, LA, GA, FL, CA, PR, PA, WV, WA, HI, NC, M
- Recall number
- FDA-Z-1223-2024
- 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.