Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2898-2020 — E.cam or Symbia systems that use foresight detectors - Product Usage: 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.

U.S. FDA — Device Enforcement · United States · 2016-03-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2898-2020
Date of alert
2016-03-31
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Medical Solutions USA, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10275007
Reported risk: E. CAM and Symbia system with foresight detectors performing gated or dynamic acquisition may lose some detector time information. Our risk analysis indicates that the probability of occurrence is remote. SPECT: 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. CT: The CT component is intended to produce cross sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial place taken at different angles or spiral planes taken at different angles. SPECT+CT: Perform CT scans and nuclear imaging studies within the same instrument. To obtain attenuation corrected images and to provide registration of anatomical and physiological images within the patient's anatomy.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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