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U.S. Department of Health and Human Services

Class 2 Device Recall GE Precision 500D

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  Class 2 Device Recall GE Precision 500D see related information
Date Initiated by Firm January 02, 2008
Date Posted September 19, 2008
Recall Status1 Terminated 3 on December 10, 2011
Recall Number Z-1610-2008
Recall Event ID 49467
510(K)Number K011624  
Product Classification Fluoroscopic X-Ray System - Product Code JAA
Product GE Precision 500D, model 2288798, 2289299, 2290479, 2305472, 2305473, 2305495, 2336900, 2345243, 2401181, 2403790, 2403791, 2404103, 2407276, 2407576, 5179385, 2289299-2, 2290479-2, 2345260-12, 2345260-3, 2403790-3, and 2403791-3, GE Medical Systems - Americas: Milwaukee, USA. The device is used to perform fluoroscopic examination of human anatomy.
Code Information serial numbers: 00000004108GQ7, 00000004874GQ4, 00000006742GQ1, 00000007111GQ8, 00000008717GQ1, 00000008892GP2, 00000010136GQ0, 00000012808GP2, 00000013547GP5, 00000013737GP2, 00000013844GP6, 00000985953WK9, 00000987224WK3, 00000987333WK2, 00000989376WK9, 00012966GP8000, 00000000BRBGDM, 00000000BRBGDR, 00000000BRBUF8, 00000000BRD138, 00000000BRF490, 00000000BRF49B, 00000000BRBBXV, 00000000BRBL7V, 00000000BRETRE, 00000986515WK5, 00000097958WK2, 000000980212WK, 00000098186WK0, 00000098235WK4, 00000098734WK5, 00000970756WK3, 00000971704WK2, 00000972504WK5, 00000972505WK2, 00000972772WK8, 00000973070WK6, 00000973500WK2, 00000973502WK8, 00000973616WK6, 00000973617WK4, 00000973618WK2, 00000973624WK0, 00000973883WK2, 00000973884WK0, 00000973885WK7, 00000974085WK3, 00000974087WK9, 00000974410WK3, 00000974411WK1, 00000974412WK9, 00000974445WK9, 00000974446WK7, 00000974447WK5, 00000974676WK9, 00000974677WK7, 00000974678WK5, 00000975166WK0, 00000975167WK8, 00000975169WK4, 00000975171WK0, 00000975172WK8, 00000975626WK3, 00000975627WK1, 00000975628WK9, 00000975629WK7, 00000975630WK5, 00000975631WK3, 00000975632WK1, 00000975946WK5, 00000975947WK3, 00000975948WK1, 00000975949WK9, 00000975958WK0, 00000975959WK8, 00000975960WK6, 00000975961WK4, 00000975962WK2, 00000975964WK8, 00000977046WK2, 00000977047WK0, 00000977048WK8, 00000977049WK6, 00000977050WK4, 00000977051WK2, 00000977052WK0, 00000977053WK8, 00000977054WK6, 00000977055WK3, 00000977233WK6, 00000977234WK4, 00000977236WK9, 00000977238WK5, 00000977239WK3, 00000977853WK1, 00000977854WK9, 00000977855WK6, 00000977857WK2, 00000977858WK0, 00000977859WK8, 00000977860WK6, 00000977861WK4, 00000978079WK2, 00000978080WK0, 00000978082WK6, 00000978083WK4, 00000978084WK2, 00000978085WK9, 00000978086WK7, 00000978485WK1, 00000978486WK9, 00000978487WK7, 00000978488WK5, 00000978489WK3, 00000978490WK1, 00000978491WK9, 00000978492WK7, 00000978493WK5, 00000978494WK3, 00000978715WK1, 00000978716WK9, 00000978826WK6, 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Recalling Firm/
Manufacturer		 GE Healthcare
3000 N Grandview Blvd
Waukesha WI 53188-1615
For Additional Information Contact
262-544-3894
Manufacturer Reason
for Recall		 GE Healthcare was notified that 2 recently installed Precision 500D systems were not in compliance with portions of the Performance Standard for Diagnostic X-ray Equipment. X-ray production was possible from the fluoroscopic X-ray tube when the Primary Protective Barrier was not in position to intercept the X-ray beam. Users are recommended to follow good clinical standards to ensure the Image I
FDA Determined
Cause 2		 Nonconforming Material/Component
Action A Product Safety Notification letter, dated 01/09/2008 was sent to affected customers. This letter described the safety issue, affected product and safety instructions. A GE Field Engineer will schedule a field visit to affected customers to inspect and replace the park latch switch as needed.
Quantity in Commerce 2863 total (2744 US / 119 OUS)
Distribution Nationwide, Washington D.C. and Puerto Rico and OUS to include: ARGENTINA, AUSTRALIA, BRAZIL, CANADA, CHILE, DOMINICAN REPUBLIC, EGYPT, GERMANY, HONDURAS, INDIA, INDONESIA, IRELAND, JAMAICA, KOREA, KUWAIT, MALAYSIA, MEXICO, NETHERLANDS, PANAMA, RUSSIAN FEDERATION, SAUDIA ARABIA, SYRIAN ARAB REPUBLIC, TAIWAN, THAILAND, UNITED ARAB EMIRATES, and UNITED KINGDOM,
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 = JAA and Original Applicant = GE MEDICAL SYSTEMS
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