---
title: "Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2 — FDA record Z-2096-2025 | Is It on Recall"
description: "Certain Spectrum infusion pumps may have an incorrect version of software."
url: https://isitonrecall.com/recall/fda-device-z-2096-2025-baxter-sigma-spectrum-infusion-pump-v8-model-number-35700bax2/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2 — FDA record Z-2096-2025

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 20, 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**: Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2
- **Reason**: Certain Spectrum infusion pumps may have an incorrect version of software.
- **Classification**: Class I
- **Recalling firm**: Baxter Healthcare Corporation
- **Quantity**: 28 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2096-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2096-2025%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 | UDI-DI: 00085412498683; Serial Numbers: 2006307 , 2052091 , 2093765 , 2095360 , 2104302 , 2119236 , 2141815 , 2025925 , 2067699 , 2094483 , 2095541 , 2105238 , 2119436 , 2143406 , 2034297 , 2074097 , 2094580 , 2096351 , 2105769 , 2135482 , 2143684 , 2051591 , 2090658 , 2095202 , 2096856 , 2118940 , 2137976 , 2156201 |

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

## Distribution

US States: CA, FL, IL, KS, MI, MS, NY, OH, OK, and VA.

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

- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Kansas](https://isitonrecall.com/state/kansas/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [Mississippi](https://isitonrecall.com/state/mississippi/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Virginia](https://isitonrecall.com/state/virginia/)

## Dates in the source

- **Report date**: Jul 23, 2025
- **Recall initiation date**: Jun 20, 2025
- **Center classification date**: Jul 17, 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-2096-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Baxter Healthcare Corporation records](https://isitonrecall.com/brand/baxter-healthcare-corporation/)