FDA Device recall Z-2579-2018
Discovery MI Digital Ready
- FDA Device
- Class II
- terminated
- Published 2018-08-08
On 2018-08-08 the FDA classified a Class II recall of Discovery MI Digital Ready by Ge Healthcare, citing DIGITAL ReadyCT/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-2579-2018 |
| 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 Digital Ready
Reason
DIGITAL ReadyCT/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 5986030. a. Serial Number PTDMI1800003PT, System ID Number RADNETPT1839, UDI Number 01008406821209751118…Model Number 5986030. a. Serial Number PTDMI1800003PT, System ID Number RADNETPT1839, UDI Number 01008406821209751118010421PTDMI1800003PT; b. Serial Number PTDMI1800005PT, System ID Number RADNETPT1838, UDI Number 01008406821209751118010421PTDMI1800003PT; c. Serial Number PTDMI1800009PT, System ID Number 813745DMIDR2, UDI Number 01008406821209751118021921PTDMI1800009PT |
|---|
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-2579-2018%22
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