The Discovery NM/CT 570c CT Standalone Scan The Discovery NM/CT 570c hybrid system is a combination of a cardiac dedicated nuclear imaging subsystem and LightSpeed GE CT subsystem. This system is intended for cardiac Nuclear Medicine (NM) diagnostic imaging applications, head and body CT diagnostic imaging applications, as well as attenuation correction and anatomical localization. The Discovery product is a SPECT-CT system. It consists of two back-to-back gantries, the NM Gantry, carrying solid state Cadmium Zinc Telluride (CZT) detectors, the CT Gantry, a single patient table, power distribution unit (PDU), NMV integrated power supply (IPS) , two operator consoles with two acquisition systems (Nuclear and CT), interconnecting cables and associated accessories (ECG gating, etc.).
FDA Recall Z-1967-2013 · Posted 2013-08-20
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Recalling FirmGE Healthcare, LLC
Recall StatusTerminated
Product CodeKPS
Date Initiated2013-04-10
Date Terminated2014-01-21
Product Quantity10 Systems
Reason for Recall
GE Healthcare has recently become aware of an incident where the wrong part of the patient body was
scanned during a CT standalone exam with the Discovery NM/CT 570c
Firm Action
GE Healthcare will remedy the issue or bring the product into compliance with each applicable Federal standard. GE Healthcare has provided field modification instructions (FMI) to update software for the Discovery NM/CT570c hybrid system. The software update will correct the incorrect positioning of the table not prescribed by the operator. The FMI includes:
A software upgrade with foreign language support to be installed in the affected models listed above,
Labels (FMI label and packing label),
Software upgrade workflow procedure with functional verification for all modes of operation, and
Certification Report, Postponement of Medical Device Correction, Rejection of Medical Device Correction, or Refusal and/or Location Unknown Documentation.
For further questions please call (262) 513-4122.
Root Cause
Radiation Control for Health and Safety Act
Distribution Pattern
US Distribution in the state of CT.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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