---
title: "BD COR System Software. Model Number: 444829. — FDA record Z-2162-2025 | Is It on Recall"
description: "Potential for functionality issue that supports the Over labeling feature and could lead to possible false negative results."
url: https://isitonrecall.com/recall/fda-device-z-2162-2025-bd-cor-system-software-model-number-444829/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# BD COR System Software. Model Number: 444829. — FDA record Z-2162-2025

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 Jun 23, 2025. 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 COR System Software. Model Number: 444829.
- **Reason**: Potential for functionality issue that supports the Over labeling feature and could lead to possible false negative results.
- **Classification**: Class II
- **Recalling firm**: Becton Dickinson & Co.
- **Quantity**: 7 systems
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2162-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2162-2025%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 | Model Number: 444829. UDI-DI: 00382904448295. Software version 8.80 and above. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide - US Nationwide distribution in the states of Florida, Texas and Michigan. The countries of Sweden and Belgium.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jul 30, 2025
- **Recall initiation date**: Jun 23, 2025
- **Center classification date**: Jul 23, 2025

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-2162-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Becton Dickinson & Co. records](https://isitonrecall.com/brand/becton-dickinson-co/)