# FDA recall Z-1992-2023

> **Draeger Medical Systems, Inc.** · Class II · device recall initiated 2023-05-16.

## Product

Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale [Model(s): RW82VHA-1, RW82VHA-1C, RW82VHA-1D, RW82-1, RW82-1C, RW82-1D, WBR82-1 and WBR82-1C]

## Reason for recall

The Resuscitaire Infant Radiant Warmer with the optional scale could display inaccurate weight values.

## Distribution

US Nationwide distribution including in the states of AL, AR, AZ, CA, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO MS, MT, NC, NE, NH, NJ, NV, NY, OH, OR, PA, PR, SD, TN, TX, VT, WA, and WI.

## Key facts

- **Recall number:** Z-1992-2023
- **Recalling firm:** Draeger Medical Systems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-16
- **Report date:** 2023-06-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Telford, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1992-2023

## Citation

> AI Analytics. FDA recall Z-1992-2023. Retrieved 2026-08-01 from https://api.ai-analytics.org/recall/Z-1992-2023. Source: US FDA. Licensed CC0.

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