CareFusion 303, Inc. 2023-10-04 Health serious FDA
Health · FDA · Recall #FDA-Z-2646-2023
BD Pyxis MedBank MedPass Software, REF: 139088-01 Recall
Issued October 4, 2023 · CareFusion 303, Inc.
In October 2023, CareFusion 303, Inc. recalled the BD Pyxis MedBank MedPass Software, REF: 139088-01, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is still available for dispense, which could lead to duplicate medication administration.
What you should do
- 1 Stop using BD Pyxis MedBank MedPass Software, REF: 139088-01 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
- October 4, 2023
- Units affected
- Not reported
- Sold at
- US: FL, MI, KS
- Recall number
- FDA-Z-2646-2023
- 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 903rd Health recall we've logged in 2023.