Discovery NM/CT 670 DR — Class II medical device recall Z-0606-2019
Completed recall by GE Healthcare, LLC, reported 2018-12-19, distributed in CA, DC, OH, UT, WI. When your system was installed, the Main disconnect switch, EPO button on the A1 panel, and Remote EPO button(
| Recall number | Z-0606-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, LLC, Waukesha, WI, United States |
| Recall initiated | 2018-05-24 |
| Classified | 2018-12-13 |
| Reported by FDA | 2018-12-19 |
| Distributed | CA, DC, OH, UT, WI |
| Countries outside the US | CA |
| Quantity | 4 units |
| UPC / GTIN / UDI-DI | 00840682124393 |
| Serial numbers | DDRW34032, DDRX34038, DDRX34041, DDRX34045 |
| Model numbers | 5376204-70-56 |
Product
Discovery NM/CT 670 DR, model 5376204-70-56 intended for use in detecting, localizing, diagnosing of diseases and organ function for the evaluation of diseases, trauma, abnormalities, and disorders such as, but not limited to, cardiovascular disease, neurological disorders and cancer.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0606-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.