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Philips Medical Systems, Inc. recalls Philips DuraDiagnost X-Ray system, Stationary X-Ray System Radiographic Models: 712210, 712211
Recalled March 18, 2015 · FDA recall Z-1251-2015 · Philips Medical Systems
Hazard
Improper installation of Tube arm, and Wall stand may cause it to fall down, Improper installation of table may cause it to float. · FDA Class II
Units
71 units
Sold at
Worldwide Distribution. Argentina, Australia, Burkina-Faso, Chile, China, Colombia, Ecuador, France, Germany, Hungary, Indonesia, Iraq (NL), Kuwait, Libya, Macedonia, Malaysia, Mayotte, Poland, Saudi Arabia, Slovenia, Spain, Switzerland, Turkey, United Kingdom, and Uzbekistan.
Description
Improper installation of Tube arm, and Wall stand may cause it to fall down, Improper installation of table may cause it to float.
Product
Philips DuraDiagnost X-Ray system, Stationary X-Ray System Radiographic Models: 712210, 712211
Manufacturer(s)
Philips Medical Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →