FDA Device recall Z-2578-2018
Discovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22
- FDA Device
- Class II
- terminated
- Published 2018-08-08
On 2018-08-08 the FDA classified a Class II recall of Discovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22 by Ge Healthcare, citing some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2578-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-05-24 |
| Published | 2018-08-08 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
Discovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22
Reason
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
Identifiers
| code_info | Model Number 5432539-22. Serial Number 502674HM5 (System ID Number 510204DISCIQ); Serial Number 504305HM4 (System ID Number 219922PTIQ) |
|---|
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-2578-2018%22
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