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FDAMay 25, 2016device

BrightView XCT Upgrade Model 882454

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

The hazard

The firm became aware of an issue where during a non-Auto Body Contouring (ABC), non-circular, rel-180 scan, the detector may come in contact with the patient. The issue was caused by a software defect in the workflow setup script.

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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BrightView XCT Upgrade Model 882454 — Recall Details · AllClear