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Philips Medical Systems (Cleveland) Inc recalls Brilliance iCT
Recalled February 1, 2017 · FDA recall Z-1058-2017 · Philips Medical Systems (Cleveland)
Hazard
During a retrospective review of production documentation it was observed that the M6 Rotor Counterweight Bolt may have been improperly torqued. · FDA Class II
Units
1-unit
Sold at
Product was not distributed in the US. Unit was distributed in Australia.
Description
During a retrospective review of production documentation it was observed that the M6 Rotor Counterweight Bolt may have been improperly torqued.
Product
Brilliance iCT
Manufacturer(s)
Philips Medical Systems (Cleveland) Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →