Events

Recall of Device Recall Mobilett XP

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Siemens Medical Solutions USA, Inc.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    37698
  • Event Risk Class
    Class 2
  • Event Number
    Z-0749-2007
  • Event Initiated Date
    2007-03-21
  • Event Date Posted
    2007-04-19
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2007-08-07
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=51335
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    mobile X-ray system - Product Code IZL
  • Reason
    Mounting bolts for tank fork assembly and collimator flange may become loose.
  • Action
    Siemens Service Personnel are visiting each consignee, beginning March 21, 2007, to replace the required mounting bolts and tighten them according to required torque specifications.

Device

Device Recall Mobilett XP
  • Model / Serial
    Serial numbers 1109, 1153, 1205, 2128, 1075, 1315, 1316, 1335, 1130, 1281, 1282, 1176, 1339, 1224, 1301, 2008, 1021, 1154, 1180, 1181, 1009, 1189, 1211, 1212, 2003, 2010, 1341, 1342, 2049, 2077, 2108, 1314, 1334, 1192, 1213, 1043, 1126, 1135, 2047, 2090, 2123, 1024, 1031, 1034, 1035, 1111, 2004, 1113, 1178, 1240, 1261, 2040, 1058, 1115, 1159, 1203, 1247, 1309, 1345, 2032, 1010, 1049, 1151, 1297, 1298, 2051, 1206, 1218, 1238, 1332, 1333, 2034, 2035, 2065, 1138, 1299, 1300, 2020, 2021, 2022, 2052, 2017, 2027, 1086, 1029, 1145, 1027, 1164, 1234, 2115, 1110, 1152, 1156, 1235, 1089, 1022, 1241, 1254, 1286, 1073, 1079, 1084, 1131, 1165, 1208, 2028, 2120, 2124, 2132, 1037, 1045, 1185, 1251, 1252, 1259, 1294, 1295, 2048, 1025, 1087, 1146, 1173, 1186, 1187, 1198, 1199, 1258, 1275, 1307, 2009, 1042, 1060, 1076, 1092, 1228, 1229, 1230, 1231, 1239, 1246, 1078, 2080, 2109, 2113, 1088, 1103, 1049, 1040, 1055, 1059, 1090, 1177, 1204, 1210, 1214, 1216, 1263, 1284, 1285, 1289, 1290, 1306, 1308, 2029, 2041, 2042, 2075, 2099, 2110, 1023, 1050, 1267, 1336, 1277, 1278, 1279, 1280, 2093, 1028, 1080, 1217, 1349, 1136, 1137, 1143, and 2100.
  • Product Classification
    Radiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    The products were shipped to medical facilities nationwide.
  • Product Description
    Mobilett XP, mobile X-ray system, Model number 1818454
  • Manufacturer
    Siemens Medical Solutions USA, Inc

Manufacturer

Siemens Medical Solutions USA, Inc
  • Manufacturer Address
    Siemens Medical Solutions USA, Inc, 51 Valley Stream Pkwy, Malvern PA 19355-1406
  • Manufacturer Parent Company (2017)
    Siemens Ag
  • Source
    USFDA