PlainRecalls
FDA Devices Moderate Class II Terminated

Revolution EVO 3.6, labeled as a. HVY WAUK; b. LONG HINO; c. LONG WAUK; d. MID BJG; e. MID WAUK.

Reported: August 8, 2018 Initiated: May 24, 2018 #Z-2584-2018

Product Description

Revolution EVO 3.6, labeled as a. HVY WAUK; b. LONG HINO; c. LONG WAUK; d. MID BJG; e. MID WAUK.

Reason for Recall

Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).

Details

Recalling Firm
GE Healthcare, LLC
Units Affected
42 units total
Distribution
Nationwide distribution to AL, CA, CO, FL, IL, IN, MA, MD, MI, MS, NC, NJ, NY,OH, OK, SC, TN, TX, VA.
Location
Waukesha, WI

Frequently Asked Questions

What product was recalled?
Revolution EVO 3.6, labeled as a. HVY WAUK; b. LONG HINO; c. LONG WAUK; d. MID BJG; e. MID WAUK.. Recalled by GE Healthcare, LLC. Units affected: 42 units total.
Why was this product recalled?
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
Which agency issued this recall?
This recall was issued by the FDA Devices on August 8, 2018. Severity: Moderate. Recall number: Z-2584-2018.