# FDA recall Z-1503-2023

> **Spacelabs Healthcare, Inc.** · Class II · device recall initiated 2023-04-12.

## Product

Ultraview SL (UVSL) Command Module, Model 91496

## Reason for recall

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.

## 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.

## Key facts

- **Recall number:** Z-1503-2023
- **Recalling firm:** Spacelabs Healthcare, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-04-12
- **Report date:** 2023-05-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Snoqualmie, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1503-2023

## Citation

> AI Analytics. FDA recall Z-1503-2023. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1503-2023. Source: US FDA. Licensed CC0.

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