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Philips Medical Systems (Cleveland) Inc recalls BrightView SPECT, Model Number 882480
Recalled July 31, 2019 · FDA recall Z-2009-2019 · Philips Medical Systems (Cleveland)
Hazard
An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released. · FDA Class II
Units
696
Sold at
Worldwide Distribution - US Nationwide
Description
An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.
Product
BrightView SPECT, Model Number 882480
Manufacturer(s)
Philips Medical Systems (Cleveland) Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →