medical MODERATE Updated 2023-06-28

Draeger Medical Systems, Inc. recalls Draeger Softbed Resuscitaire and/or Birthing Room Warmer wit

See all recalls from Draeger Medical Systems, Inc. →

Recalled 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]

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: All units shipped from January 20, 2020 through March 1, 2023; MU20503 (Resuscitaire) UDI - 04049098000215 MU20512 (Birthing Room Warmer - BRW) UDI - 04049098058001

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Draeger Softbed Resuscitaire and/or →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

Baxter Healthcare Corporation recalls Brand Name: Exacta Mix Product Name: Vented Micro-Volume In

2026-06-10 · Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow efficiency, incomplete or slower transfers of ingredients, or system alarms. This issue may lead to clinical effects such as electrolyte imbalance, metabolic instability, delayed recovery, etc.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion 5M12, Model Numbers: 722227 with Software r

2026-06-10 · During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.

B Braun Medical Inc recalls Design Options Spinal Tray Spinal Needle Anesthesia procedur

2026-06-10 · These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.

CareFusion 303, Inc. recalls BD Pyxis MedStation ES Tower REF: 352 Medication cabinet

2026-06-10 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn.