FDA Device recall Z-2758-2016
e.cam and Symbia E gamma camera systems with patient beds To detect or image the distribution of radionuclides in the body or organ, using…
- FDA Device
- Class II
- terminated
- Published 2016-09-14
On 2016-09-14 the FDA classified a Class II recall of e.cam and Symbia E gamma camera systems with patient beds To detect or image the distribution of radionuclides in the body or organ, using… by Siemens Medical Solutions Usa, citing "We have received reports of patients hair being caught in the e.cam and Symbia E patient bed up/down drive. The purpose of this letter is to remind users of the patient position….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2758-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-08-05 |
| Published | 2016-09-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
e.cam and Symbia E gamma camera systems with patient beds 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.
Reason
"We have received reports of patients hair being caught in the e.cam and Symbia E patient bed up/down drive. The purpose of this letter is to remind users of the patient positioning instructions for your e.cam or Symbia E system and to inform you of an update that will be performed by your local Siemens service representative."
Identifiers
| code_info | Model numbers 4380213, 4380221, 5242826, 5977066, 5977074, 5984005, 5989079, 5989087, 5989095, 5991109, 5991117, 599209…Model numbers 4380213, 4380221, 5242826, 5977066, 5977074, 5984005, 5989079, 5989087, 5989095, 5991109, 5991117, 5992099, 7324119, 7324135, 7324143, 7324150, 7760809, 7760932, 7761161, 7823920, 7823938, 7823946, 7823953, 7823961, 7823979, 10151531, 10151532, 10275879, 10413009, 10520745. Serial numbers: 2005003 , 5130 , 1176 , 1180 , 1161 , 1169 , 1162 , 1163 , 1165 , 1166 , 1172 , 2025 , 2052 , 7595 , RC524 , RC495 , 8515 , 1198 , 1202 , 10016 , 5563 , 5556 , 7588 , 8757 , 10342 , 11371 , 11666 , 5560 , 7507 , 7596 , 10345 , 11674 , 1210 , 1211 , 1005 , 1156 , 1261 , 5562 , 5538 , 5555 , 10348 , 11372 , 1155 , 4019 , 8545 , 8756 , 9241 , 9235 , 9238 , 10351 , 10346 , 10350 , 11370 , 1262 , 1028 , 1358 , 4112 , 7509 , 7606 , 7599 , 8760 , 8758 , 1209 , 1208 , 1032 , 7600 , 8759 , 9173 , 9245 , 1213 , 5561 , 5514 , 7608 , 8761 , 1212 , 1359 , 1075 , 4117 , 7605 , 8763 , 8767 , 9240 , 9243 , 10356 , 1 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2758-2016%22
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