Discovery NM/CT 670 Pro recall
Discovery NM/CT 670 Pro, model 5376204-70-54
Why was Discovery NM/CT 670 Pro 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
GTIN 00840682121194 Serial Number ESDX35015
- Product
- Discovery NM/CT 670 Pro, model 5376204-70-54
- Recalling firm
- GE Healthcare, LLC
- Quantity
- 1 unit
- Distribution
- CA, DC, OH, UT, WI, Canada
- Recall date
- December 19, 2018
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (device)