---
title: "BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions — FDA record Z-2179-2025 | Is It on Recall"
description: "Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream"
url: https://isitonrecall.com/recall/fda-device-z-2179-2025-bd-alaris-pump-module-model-8100-with-guardrails-suite-mx-software-versions/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions — FDA record Z-2179-2025

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 Jul 8, 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 Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions
- **Reason**: Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.
- **Classification**: Class I
- **Recalling firm**: CareFusion 303, Inc.
- **Quantity**: 33,162,680 units total
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2179-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2179-2025%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 | BD Alaris" Pump Module Model 8100- All Serial Numbers/ UDI(s): 10885403222054, 10885403517723, 10885403810015, 10885403810039, 10885403810046 |

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

## Distribution

US Nationwide Distribution to states of: AK AL AR AS AZ CA CO CT DC DE FL GA GU HI IA ID IL IN KS KY LA MA MD ME MI MN MO MP MS MT NC ND NE NH NJ NM NV NY OH OK OR PA PR RI SC SD TN TX UT VA VT WA WI WV WY; and OUS (foreign) to countries of: Japan, Italy, Germany, Turkey

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

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

## Dates in the source

- **Report date**: Aug 13, 2025
- **Recall initiation date**: Jul 8, 2025
- **Center classification date**: Aug 6, 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-2179-2025%22)

## Related records

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