FDAApril 7, 2020device

Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model: 720013 - Product Usage: general radiography.

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

The hazard

If the shaft breaks due to material fatigue, the trauma arm can fall down and may result in injury.

What to do

FDA enforcement status: Terminated

Brands named

philips north americaphilipsphilips north

Recall history

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

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