FDA Device recall Z-2580-2018
Discovery MI, labeled as Discovery DMI 15 cm 3 ring, and Discovery DMI 20cm 4 ring
- FDA Device
- Class II
- terminated
- Published 2018-08-08
On 2018-08-08 the FDA classified a Class II recall of Discovery MI, labeled as Discovery DMI 15 cm 3 ring, and Discovery DMI 20cm 4 ring 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-2580-2018 |
| 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 MI, labeled as Discovery DMI 15 cm 3 ring, and Discovery DMI 20cm 4 ring
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 5454001-170. Serial Number (System ID Number): CJRPX1800016CN ( 4550966PT11), CJRPX1800017CN (561422MI…Model Number 5454001-170. Serial Number (System ID Number): CJRPX1800016CN ( 4550966PT11), CJRPX1800017CN (561422MI), CJRPX1800018CN (617726PET1EB), CJRPX1800021CN (404616DMI) |
|---|
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-2580-2018%22
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