The Recall Desk
HighFDA (Devices)·Z-0484-2019·Announced 2018-11-28

GE Healthcare Panda Wall Mount Infant Radiant Warmer Recalled for Electric Leakage

GE Healthcare is recalling 1,724 Panda Wall Mount infant radiant warmers worldwide due to a potential electric leakage hazard that could affect users.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a risk-of-harm product (electric leakage) where injury has not yet been reported, which aligns with the High severity criteria in the rubric.

Plain-English summary

GE Healthcare, LLC is recalling 1,724 units of the Panda Wall Mount infant radiant warmer. The recall is being conducted because of a potential electric leakage issue that could affect the user. The devices are distributed worldwide, including in the United States and numerous international locations.

The affected devices are identified by Model Number 2063570-001-149242 and UDI (Serial Number) HDJU65781. The recall is classified as Class II by the U.S. Food and Drug Administration. No specific dates or additional distribution details are provided in the source text.

Consumers and healthcare facilities should contact GE Healthcare, LLC for instructions on how to address the potential electric leakage hazard. The source text does not specify a particular action such as stopping use or returning the device, but users should follow the recalling firm's guidance.

The recalled product

Product
Panda Wall Mount warmer. Infant radiant warmer
Manufacturer
GE Healthcare, LLC
Category
Medical Device — Infant Radiant Warmer
Hazard
Affected units
1,724

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (3)

  • Model Number
  • UDI (Serial Number): 2063570-001-149242
  • Not Applicable (HDJU65781)

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 6 recalled by GE Healthcare, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 6 products in this recall →

Related recalls

Same manufacturer · GE Healthcare, LLC

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Same hazard · electric leakage

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