GE OEC Medical Systems, Inc


   04 رجب 1428 هـ الموافق 18 يوليو 2007 م
Recalling Firm / Manufacturer GE OEC Medical Systems, Inc
Product GE OEC 9900 Elite Fluoroscopic X-ray System, GE Healthcare, Salt Lake City, Utah.
Code Information Serial numbers: E2-0155, E2-0156, E2-0157, E2-0164, E2-0167, E2-0168, E2-0170 thru E2-0234, E2-0235-C, E2-0236 thru E2-0257, E2-0259, E2-7048-MH, E2-7050-MH, E2-7051-MH, E2-7058-MH, E2-7059-MH, E2-7060-MH, E2-7061-MH, E2-7062-MH, E2-7064-MH, E2-7065-MH, E2-7066-MH, E2-7067-MH, E2-7068-MH, E2-7069-CMH, E2-7070-MH, E2-7071-MH, E2-7072-MH, E2-7073-MH, E2-7074-MH, E2-7076-MH, E2-7077-CMH, E9-0037, E9-0085, E9-0088, E9-0089-G, E9-0090, E9-0093, E9-0094, E9-0095, E9-0098 thru E9-0103, E9-0108 thru E9-0153, E9-0155, E9-0156, E9-0157, E9-0158, E9-0159, E9-0162, E9-0163, E9-0164, E9-0165, E9-0170, E9-0171, E9-0172, E9-0173, E9-0178, E9-0183, ES-0041-G, ES-0069, ES-0071, ES-0072, ES-0078, ES-0084-G, ES-0086-G, ES-0087, ES-0088, ES-0089, ES-0090, ES-0092-CH, ES-0096, ES-0097, ES-0098, ES-0099-CH, ES-0101-CH, ES-0103, ES-0104, ES-0106 thru ES-0130, ES-0131-H, ES-0132 thru ES-0154, ES-0155-H, ES-0156, ES-0157, ES-0158, ES-0159, ES-0160, ES-0162-G thru ES-0167-G, ES-0169-CH, ES-0170, ES-0171, ES-0172, ES-0173, ES-0175, ES-0176, ES-0177, ES-0178, ES-0184, ES-7018-MH, ES-7026-CMH thru ES-7031-CMH, ES-7032-MH, ES-7033-CMH, ES-7034-CMH, ES-7035-CMH, ES-7036-CMH.
Reason of Recall X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.
Date Recall Initiated June 12, 2007
Action Consignees were notified by letter on 06/12/2007 and told that a service representative would arrange for an inspection and would modify their systems. Firm Initiated recall is ongoing.
Contact GE Healthcare
01 / 4600530
Source of Information U.S. FDA
SFDA Comments SFDA urges all hospitals that have devices subjected to recall, to contact the company.