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GE Healthcare, LLC recalls VariCam
Recalled January 16, 2019 · FDA recall Z-0704-2019 · GE Healthcare
Hazard
A potential hazardous situation may occur if the collimator locking handle is not properly placed in the lock position and the warning circuit does not detect that the collimator is unlocked because of the patient proximity to the collimator during a clinical scan. · FDA Class II
Units
64 units
Sold at
Worldwide
Description
A potential hazardous situation may occur if the collimator locking handle is not properly placed in the lock position and the warning circuit does not detect that the collimator is unlocked because of the patient proximity to the collimator during a clinical scan.
Product
VariCam
Manufacturer(s)
GE Healthcare, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →