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U.S. Department of Health and Human Services

Class 2 Device Recall Innova 2000 and Innova 2000 S; and Innova 2000 and Innova 2000S mobile version

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  Class 2 Device Recall Innova 2000 and Innova 2000 S; and Innova 2000 and Innova 2000S mobile version see related information
Date Initiated by Firm March 06, 2006
Date Posted May 24, 2006
Recall Status1 Terminated 3 on February 24, 2008
Recall Number Z-0896-06
Recall Event ID 34758
510(K)Number K022322  K024200  
Product Classification Solid State X-Ray Imager (Flat Panel/Digital Imager) - Product Code MQB
Product GE Medical Systems Innova 2000 and Innova 2000S, and Innova 2000 and Innova 2000S mobile version. Cardiovascular Imaging System.
Code Information all serial numbers
Recalling Firm/
Manufacturer		 GE Healthcare
3000 N Grandview Blvd
Waukesha WI 53188-1615
For Additional Information Contact
262-544-3894
Manufacturer Reason
for Recall		 Incorrect screws were used for mounting the detector which may lead to a possible part falling onto a patient.
FDA Determined
Cause 2		 Other
Action GEHC is issuing a validated field action 3/6/2006 to correct the issues. Existing screws/bolts will be replaced using correct torque with screws containing cotter pins. Loctite liquid glue will be applied. Service manuals have been updated with instructions for using correct screws and torque. The field action is being implemented via Field Modification Instruction (FMI) 12033.
Quantity in Commerce 856 (534 domestic and 322 OUS)
Distribution Nationwide including Puerto Rico and OUS to include: Australia, Belgium, Brazil, Bulgaria, Byelarus, Canada, China, Columbia, Czech Republic, Denmark, Egypt, Finland, France, Georgia, Germany, Greece, Honduras, Hungary, Indonesia, Iraq, Ireland, Israel, India, Iran, Italy, Jordan, Japan, Republic of Korea, Lebanon, Lithuania, Martinique, Mexico, Morocco, Netherlands, Norway, New Zealand, Poland, Portugal, Russia, Saudi Arabia, Singapore, South Africa, Spain, Sweden, Switzerland, Syrian Arab Republic, Taiwan, Republic of China, Thailand, Tunisia, Turkey, United Kingdom, Venezuela
Total Product Life Cycle TPLC 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) Database 510(K)s with Product Code = MQB and Original Applicant = GE MEDICAL SYSTEMS, INC.
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