---
title: "BD Pyxis MedBank MedPass Software, REF: 139088-01 — FDA record Z-2646-2023 | Is It on Recall"
description: "After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is"
url: https://isitonrecall.com/recall/fda-device-z-2646-2023-bd-pyxis-medbank-medpass-software-ref-139088-01/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / 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](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## 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

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2646-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). 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.

- [Florida](https://isitonrecall.com/state/florida/)
- [Kansas](https://isitonrecall.com/state/kansas/)
- [Michigan](https://isitonrecall.com/state/michigan/)

## 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.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2646-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [CareFusion 303, Inc. records](https://isitonrecall.com/brand/carefusion-303-inc/)