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U.S. Department of Health and Human Services

Class 2 Device Recall Revolution CT 160

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 Class 2 Device Recall Revolution CT 160see related information
Date Initiated by FirmMay 24, 2018
Create DateJuly 31, 2018
Recall Status1 Terminated 3 on February 08, 2019
Recall NumberZ-2582-2018
Recall Event ID 80484
510(K)NumberK133705 K163213 
Product Classification System, x-ray, tomography, computed - Product Code JAK
ProductRevolution CT 160 1.5D STD WAUK
Code Information Model Number 5590000-6. Serial number REVVX1800021CN (System ID 812842REV, UDI 01008406821185521118020021REVVX1800021CN), Serial Number REVVX1800004CN (System ID 269375REVOCT, UDI 01008406821185521118010021REVVX1800004CN).
Recalling Firm/
Manufacturer		 GE Healthcare, LLC
3000 N Grandview Blvd
Waukesha WI 53188-1615
For Additional Information Contact
800-437-1171
Manufacturer 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).
FDA Determined
Cause 2		Component change control
ActionGE Healthcare notified customers on about 05/24/2018 via URGENT MEDICAL DEVICE CORRECTION letter. The letter outlined the reason for recall and notified customers that a GE Healthcare representative would be contacting them to arrange for the correction of the devices. Any questions or concerns can be directed to GE Healthcare Service at 1-800-437-1171 or a local Service Representative.
Quantity in Commerce42 units total
DistributionNationwide distribution to AL, CA, CO, FL, IL, IN, MA, MD, MI, MS, NC, NJ, NY,OH, OK, SC, TN, TX, VA.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = JAK
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