Z-2646-2023 Class II Ongoing
FDA device recall Z-2646-2023 was initiated by CareFusion 303, Inc. on August 18, 2023 and is designated Class II. 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 coul… The recall status is ongoing. Affected quantity: 37.
Recall Details
- Product Type
- Devices
- Report Date
- October 4, 2023
- Initiation Date
- August 18, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 37
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.
Distribution Pattern
US: FL, MI, KS
Code Information
UDI-DI: 10885403513817, Software versions prior to but not including v1.2.3.23