Recall Z-2646-2023— CareFusion 303, Inc.
Class II · Ongoing
Class II FDA medical device recall by CareFusion 303, Inc., initiated 2023-08-18. FDA's recall record names no specific 510(k) clearance for this event. Product: BD Pyxis MedBank MedPass Software, REF: 139088-01. Reason: 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..
- Recalling firm
- CareFusion 303, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-08-18
- Firm location
- San Diego, CA, United States
Product description
BD Pyxis MedBank MedPass Software, REF: 139088-01
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.