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Philips North America, LLC recalls Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model: 720013 - Product Usage: general radiography.
Recalled May 6, 2020 · FDA recall Z-1806-2020 · Philips North America
Hazard
If the shaft breaks due to material fatigue, the trauma arm can fall down and may result in injury. · FDA Class II
Units
346 units (5 US and 341 OUS)
Sold at
Worldwide distribution - US Nationwide distribution including the states of CA, ME, RI, TX, WI and the countries of Canada, Australia, Austria, France, Germany, Greece, Hungary, Ireland, Netherlands, Portugal, Slovenia, United Kingdom.
Description
If the shaft breaks due to material fatigue, the trauma arm can fall down and may result in injury.
Product
Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model: 720013 - Product Usage: general radiography.
Manufacturer(s)
Philips North America, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →