---
title: "Spacelabs Ultraview DM4 Vital Signs Monitor (all variations -M, -N, -MF, -NF,... — FDA record Z-3099-2024 | Is It on Recall"
description: "This product labeling does not adequately provide warning about the risks associated with the use of damaged batteries or batteries past the intended use life."
url: https://isitonrecall.com/recall/fda-device-z-3099-2024-spacelabs-ultraview-dm4-vital-signs-monitor-all-variations-m-n-mf-nf-mw-nw-mfw-nfw-model-number-9133/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Spacelabs Ultraview DM4 Vital Signs Monitor (all variations -M, -N, -MF, -NF, -MW, -NW, -MFW, -NFW), Model Number 91331 — FDA record Z-3099-2024

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 13, 2024. 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**: Spacelabs Ultraview DM4 Vital Signs Monitor (all variations -M, -N, -MF, -NF, -MW, -NW, -MFW, -NFW), Model Number 91331
- **Reason**: This product labeling does not adequately provide warning about the risks associated with the use of damaged batteries or batteries past the intended use life.
- **Classification**: Class II
- **Recalling firm**: Zoe Medical Incorporated
- **Quantity**: 1506 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-3099-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3099-2024%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 No. 91331-M; UDI-DI 00851920007347; all serial numbers up to GFD10486 Model No. 91331-MF; UDI-DI 00851920007354; all serial numbers up to GFD10486 Model No. 91331-N; UDI-DI 00851920007309; all serial numbers up to GFD10486 Model No. 91331-NF; UDI-DI 00851920007316; all serial numbers up to GFD10486 Model No. 91331-MW; UDI-DI 00851920007361; all serial numbers up to GFD10486 Model No. 91331-MFW; UDI-DI 00851920007378; all serial numbers up to GFD10486 Model No. 91331-NW; UDI-DI 00851920007323; all serial numbers up to GFD10486 Model No. 91331-NFW; UDI-DI 00851920007330; all serial numbers up to GFD10486 |

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

## Distribution

awaiting additional details

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Sep 18, 2024
- **Recall initiation date**: Aug 13, 2024
- **Center classification date**: Sep 10, 2024

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-3099-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Zoe Medical Incorporated records](https://isitonrecall.com/brand/zoe-medical-incorporated/)