---
title: "Ultraview SL (UVSL) Command Module, Model 91496 — FDA record Z-1503-2023 | Is It on Recall"
description: "Command modules will display the following when parameter processing is suspended, depending on software version: 1) Older versions will have waveforms present"
url: https://isitonrecall.com/recall/fda-device-z-1503-2023-ultraview-sl-uvsl-command-module-model-91496/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Ultraview SL (UVSL) Command Module, Model 91496 — FDA record Z-1503-2023

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 Apr 12, 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**: Ultraview SL (UVSL) Command Module, Model 91496
- **Reason**: Command modules will display the following when parameter processing is suspended, depending on software version: 1) Older versions will have waveforms present with no alarms, 2) Newer versions have waveforms absent with no alarms. This may cause clinicians to miss a potentially catastrophic event.
- **Classification**: Class II
- **Recalling firm**: Spacelabs Healthcare, Inc.
- **Quantity**: 1,088
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1503-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1503-2023%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 | Software version 2.03.06 and earlier and software version 2.04 and later. |

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

## Distribution

US Nationwide distribution in the states of SD, KY, MO, WA, OH, NC, CA, OR, TX, GA, IL, OK, SC, PA, AL, KS, FL, ID, MI, MN, IA, NJ, MD, VA, AR, CT, NE, LA, AK, MS, ME, WV, NY, AZ, TN, WY, IN, MA, MT, CO, DE, ND, WI, NV, RI, NH, UT.

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

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## Dates in the source

- **Report date**: May 10, 2023
- **Recall initiation date**: Apr 12, 2023
- **Center classification date**: May 3, 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-1503-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Spacelabs Healthcare, Inc. records](https://isitonrecall.com/brand/spacelabs-healthcare-inc/)
