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U.S. Department of Health and Human Services

Class 2 Device Recall OEC 7700 Mobile Fluoroscopy System

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  Class 2 Device Recall OEC 7700 Mobile Fluoroscopy System see related information
Date Initiated by Firm September 28, 2007
Date Posting Updated March 15, 2008
Recall Status1 Terminated 3 on November 01, 2011
Recall Number Z-0717-2008
Recall Event ID 46349
510(K)Number K000221  
Product Classification Mobile FluoroscopyX-Ray System - Product Code JAA
Product GE Healthcare, Mobile Fluoroscopy X-Ray System, OEC, Model 7700, GE Healthcare, Surgery, Salt Lake City, Utah
Code Information All Serial Numbers beginning with 79-, which is followed by 2006, 2008, 2009, 2011, 2013, 2014, 2015, 2016, 2018, C0513-C, C0878, C0986, C1016, C1017, C1021, C1037, C1038, C1043, C1044, C1052, C1053, C1054, C1055, C1056, C1060, C1061, C1062, C1063, C1065, C1068, C1069, C1070, C1080, C1082, C1083, C1087, C1088, C1091, C1155, C1162, C1165, C1170, C1176, C1180, C1181, C1184, C1187, C1188, C1189, C1190-M, C1192, C1193, C1195, C1196, C1197, C1198, C1199, C1201, C1203, C1204, C1207, C1208, C1209, C1210, C1212, C1213, C1214, C1216, C1219, C1236, C1238, C1241, C1246, C1248, C1249, C1254, C1255, C1259, C1260, C1263, C1265, C1266, C1269, C1271, C1272-RC, C1275, C1279, C1281, C1306, C1427, C1434, C1437, C144, C1446, C1461, C1476, C1501, C1507-M, C1511, C1529, C153, C1557, C1571, C1578, C158-RC, C1697, C1703, C1716, C1721, C1835, C1841, C1883, C189, C1903, C193, C2058, C2061, C3005, C3050, C3052a, C3053, C3055C3056, C3057, C3058, C3059, C3062, C3063, C3073, C3074, C3075, C3076, C3077, C3078, C3081, C3082, C3084, C3094, C3112, C3114, C3124, C3126, C3130, C3138, C3142, C3144, C3279, C601, C604, C605, C606-RC, C608, C609, C610, C613, C614, C616, C617, C618, C619, C620, C625, C626, C631, C633, C636, C640, C641, C647, C647-RC, C648, C651, C656, C666, C667, C669, C675, C676, C679, C680, C681, C682, C683, C684, C685, C689, C691, C692, C693, C694, C698, C699, C7084, C727, C744, C753, C774, C787, C800, C807, C808, C819, C855, C860, C863, C870, C873-RC, C878, C883-M, C886, C895-M, C904, C905, C906, C907-M, C911, C913, C916, C917-M, C922, C923-M, C926, C927, C928, C930, C933, C937, C938, C942, C943, C948, C949, C953-C, C953-M, C954, C955, C957-M, C970-M, C976, C982, C986, C987, S0607, S0970M, S1000, S1001, S1020, S1024, S1058, S1059, S1071, S1077, S1078, S1098, S1108, S1145, S1169-M, S1221-M, S1287, S1322, S1497, S1545, S1581, S1686, S271, S300, S418, S605, S615, S621, S622, S627, S628, S629, S630, S632, S634, S635, S637, S638, S639, S643, S644, S645, S646, S649, S649a, S650, S652, S653, S655, S657, S658, S659, S660, S661, S662, S663, S664, S668, S670, S671, S672, S674, S676, S677, S678, S686, S687, S696, S699, S700, S705, S732, S738, S746, S748, S766, S773, S779S766-RC, S791, S792, S798, S805-RC, S806, S814, S815, S816, S817, S818, S823, S824, S825, S829, S831, S838, S843, S845, S846, S846-M, S853, S854, S858, S859, S862, S863, S865-M, S867, S869, S874, S875, S879, S882, S884, S885-M, S891, S896, S900, S901, S901-M, S959, S964, S965, S969, S981, S988, S992, and S997.
Recalling Firm/
GE OEC Medical Systems, Inc
384 Wright Brothers Dr
Salt Lake City UT 84116-2862
For Additional Information Contact
Manufacturer Reason
for Recall
Unnecessary operator exposure; X-ray machine may allow unwanted x-ray exposure to the operator.
FDA Determined
Cause 2
Action On or about 9/6/2007, by Customer Notification Letter, users were notified that all affected units will be corrected by GE personnel with the addition of an additional shield.
Quantity in Commerce 309 systems (Domestic), 101 (Foreign)
Distribution Worldwide- USA including states of CO, DE, FL, NJ, MO, NY, PA, and TX (with VA and Military facilities) and countries of Australia, Austria, Belgium, Brazil, Chile, China, The Czech Republic, Denmark, France, Germany, Hungary, Israel, Italy, Norway, Spain, Sweden, Switzerland, Thailand, and The UK.
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 DEC MEDICAL SYSTEMS