Discovery NM/CT 670 Pro, model 5376204-70-54
Reported: December 19, 2018 Initiated: May 24, 2018 #Z-0608-2019
Product Description
Discovery NM/CT 670 Pro, model 5376204-70-54
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.
Details
- Recalling Firm
- GE Healthcare, LLC
- Units Affected
- 1 unit
- Distribution
- CA, DC, OH, UT, WI, Canada
- Location
- Waukesha, WI
Frequently Asked Questions
What product was recalled? ▼
Discovery NM/CT 670 Pro, model 5376204-70-54. Recalled by GE Healthcare, LLC. Units affected: 1 unit.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 19, 2018. Severity: Moderate. Recall number: Z-0608-2019.
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