Recall archive / FDA device enforcement
BD Pyxis MedBank MedPass Software, REF: 139088-01 — FDA record Z-2646-2023
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Aug 18, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- 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.
- Classification
- Class II
- Recalling firm
- CareFusion 303, Inc.
- Quantity
- 37
- Agency-reported status
- Ongoing
- Source record identifier
- Z-2646-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI-DI: 10885403513817, Software versions prior to but not including v1.2.3.23 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US: FL, MI, KS
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Oct 4, 2023
- Recall initiation date
- Aug 18, 2023
- Center classification date
- Sep 28, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.