# FDA recall Z-0481-2019

> **GE Healthcare, LLC** · Class II · device recall initiated 2018-09-25.

## Product

Giraffe Warmer. Device sold under the following product names: Giraffe Warmer and Giraffe Bedded Warmer.   infant radiant warmer.

## Reason for recall

Potential electric leakage affecting the user.

## Distribution

Worldwide distribution. US Nationwide, Algeria, Australia, Austria, Belgium, Canada, Chile, China, Costa Rica, Cyprus, Czech Republic, Denmark, Finland, France, Germany, Honduras, India, Indonesia, Ireland, Italy, Japan, Kazakhstan, Korea, Lithuania, Mexico, Netherlands, New Zealand, Norway, Pakistan, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Tanzania, Thailand, Turkey, United Arab Emirates, United Kingdom, Vietnam.

## Key facts

- **Recall number:** Z-0481-2019
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-09-25
- **Report date:** 2018-11-28
- **Termination date:** 2020-07-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0481-2019

## Citation

> AI Analytics. FDA recall Z-0481-2019. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0481-2019. Source: US FDA. Licensed CC0.

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