RecallRadar

FDA Device recall Z-0914-2015

e.cam -emission computed tomography system Used to detect or image the distribution of radionuclides in the body or organ, using the follow…

On 2015-01-14 the FDA classified a Class II recall of e.cam -emission computed tomography system Used to detect or image the distribution of radionuclides in the body or organ, using the follow… by Siemens Medical Solutions Usa, citing there is a potential for patient finger injury on the e.cam systems.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0914-2015
ClassificationClass II
Statusterminated
Initiated2014-04-08
Published2015-01-14
Last updated2026-09-13 11:53 UTC
CompanySiemens Medical Solutions Usa
DistributionUS

Product

e.cam -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 588keV.

Reason

There is a potential for patient finger injury on the e.cam systems.

Identifiers

code_info
1) E.CAM DCR Duet Head, A (e.soft); Serial Numbers: 7090 , 7501 , 7502 , 8001 , 8002 , 8003 , 8004 , 8501 , 850…1) E.CAM DCR Duet Head, A (e.soft); Serial Numbers: 7090 , 7501 , 7502 , 8001 , 8002 , 8003 , 8004 , 8501 , 8502 , 8506 , 8507 ; 2) E.CAM DCR Gantry Dual Head, Bl Serial Numbers: 3097 , 8502 , 8507 , 8508 , 8509 , 8510 , 8511 , 8514 , 8516 , 8521 , 8522 , 9821 , 71101 ; 3) E.CAM DCR Gantry Single Head; Serial Numbers: 5045 , 7501 , 7502 , 7503 , 7504 , 7505 , 7506 , 7507 , 7508 , 7509 , 7510 , 7511 , 7512 , 8001 , 8002 , 8003 , 8004 , 8005 , 8006 , 8007 , 8008 , 8009 , 8010 , 8011 , 8012 , 8013 , 8014 , 8015 , 8016 , 8017 , 8018 , 8019 , 8020 , 8021 , 8022 , 8023 , 8024 , 8025 , 8026 , 8027 , 8028 , 8029 , 8030 , 8031 , 8032 , 8033 , 8501 , 8502 , 8503 , 8504 , 8505 , 8506 , 8507 , 8508 , 8509 , 8510 , 8511 , 8512 , 8513 , 8514 , 8516 , 8517 , 8518 , 8519 , 8520 , 8521 , 8522 , 8523 , 8524 , 8525 , 8526 , 8527 , 8528 , 8530 , 8532 , 8533 , 8534 , 8535 , 8536 , 8537 , 8538 , 8539 ,

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-0914-2015%22

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