FDA Device recall Z-0484-2019
Panda Wall Mount warmer
- FDA Device
- Class II
- terminated
- Published 2018-11-28
On 2018-11-28 the FDA classified a Class II recall of Panda Wall Mount warmer by Ge Healthcare, citing potential electric leakage affecting the user.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0484-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-09-25 |
| Published | 2018-11-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
Panda Wall Mount warmer. Infant radiant warmer
Reason
Potential electric leakage affecting the user.
Identifiers
| code_info | Model Number, UDI (Serial Number): 2063570-001-149242, Not Applicable (HDJU65781); |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0484-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.