# FDA recall Z-0607-2019

> **GE Healthcare, LLC** · Class II · device recall initiated 2018-05-24.

## Product

Discovery NM/CT 670 ES, model 5376204-70-57

## 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.

## Distribution

CA, DC, OH, UT, WI, Canada

## Key facts

- **Recall number:** Z-0607-2019
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2018-05-24
- **Report date:** 2018-12-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0607-2019

## Citation

> AI Analytics. FDA recall Z-0607-2019. Retrieved 2026-07-01 from https://api.ai-analytics.org/recall/Z-0607-2019. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*