FDA Device recall Z-0607-2019
Discovery NM/CT 670 ES, model 5376204-70-57
- FDA Device
- Class II
- completed
- Published 2018-12-19
On 2018-12-19 the FDA classified a Class II recall of Discovery NM/CT 670 ES, model 5376204-70-57 by Ge Healthcare, citing when your system was installed, the Main disconnect switch, EPO button on the A1 panel, and Remote EPO button(s) (outside of the A1 panel) may not have been wired correctly which….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0607-2019 |
| Classification | Class II |
| Status | completed |
| Initiated | 2018-05-24 |
| Published | 2018-12-19 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Healthcare |
| Distribution | CA, DC, OH, UT, WI |
Product
Discovery NM/CT 670 ES, model 5376204-70-57
Reason
When your system was installed, the Main disconnect switch, EPO button on the A1 panel, and Remote EPO button(s) (outside of the A1 panel) may not have been wired correctly which could result in these not shutting off all power to the entire system as intended, resulting in a potential electric hazard.
Identifiers
| code_info | GTIN 00840682123877 Serial Numbers: ESDX35013, ESDW35010 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: completed.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0607-2019%22
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