FDAJune 10, 2019device

BrightView XCT , Model Number 882482

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.

What to do

FDA enforcement status: Terminated

Brands named

philips medical systems clevelandphilipsphilips medical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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