FDA Device recall Z-2043-2014
Symbia E camera system
- FDA Device
- Class II
- terminated
- Published 2014-07-23
On 2014-07-23 the FDA classified a Class II recall of Symbia E camera system by Siemens Medical Solutions Usa, citing siemens Medical Solutions USA, Inc. has received reports indicating the collimator cart rear casters may become loose.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2043-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-23 |
| Published | 2014-07-23 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Symbia E camera system. Emission Computed Tomography System used to detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588 keV. Nuclear medicine diagnostic device.
Reason
Siemens Medical Solutions USA, Inc. has received reports indicating the collimator cart rear casters may become loose.
Identifiers
| code_info | 1) Symbia E Dual Head System; Model Number: 10275879; Serial Numbers: 1066 ; 1090 ; 1184 ; 1185 ; 1552 ; 1443 ; 1…1) Symbia E Dual Head System; Model Number: 10275879; Serial Numbers: 1066 ; 1090 ; 1184 ; 1185 ; 1552 ; 1443 ; 1442 ; 1479 ; 1500 ; 1505 ; 1519 ; 1534 ; 1535 ; 1539 ; 1546 ; 1554 ; 1559 ; 1562 ; 1064 ; 1060 ; 1520 ; 1042 ; 1127 ; 1553 ; 1225 ; 1228 ; 1488 ; 1446 ; 1461 ; 1232 ; 1480 ; 1494 ; 1029 ; 1292 ; 1234 ; 1106 ; 1014 ; 1329 ; 1027 ; 1324 ; 1072 ; 1319 ; 1487 ; 1462 ; 1538 ; 1339 ; 1200 ; 1213 ; 1345 ; 1241 ; 1142 ; 1557 ; 1273 ; 1124 ; 1101 ; 1216 ; 1532 ; 1337 ; 1013 ; 1131 ; 1367 ; 1468 ; 1026 ; 1043 ; 1056 ; 1107 ; 1108 ; 1111 ; 1133 ; 1211 ; 1217 ; 1271 ; 1277 ; 1311 ; 1312 ; 1333 ; 1356 ; 1392 ; 1451 ; 1454 ; 1455 ; 1467 ; 1471 ; 1491 ; 1540 ; 1541 ; 1004 ; 1248 ; 1055 ; 1048 ; 1434 ; 1236 ; 1238 ; 1235 ; 1237 ; 1208 ; 1363 ; 1341 ; 1412 ; 1464 ; 1435 ; 1453 ; 1199 ; 1075 ; 1198 ; 1197 ; 1161 ; 1162 ; 1041 ; 1040 ; 1050 ; 1394 ; 1207 ; 1146 ; 1218 ; 1139 ; 11 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2043-2014%22
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