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Philips North America, LLC recalls Philips Zenition 70, System code 718133 - Product Usage: The devices are used for radiological guidance and visualizatio

Recalled May 20, 2020 · FDA recall Z-1933-2020 · Philips North America

Hazard
When strain relief is lost at the stand side of the Stand MVS Trolley Cable, over time one or more electrical contacts could break due to pulling, twisting, or dropping of the connector. If this happens, live parts may be exposed (230 V) and/or the video signal can be lost. · FDA Class II
Units
25 total
Sold at
Worldwide distribution - US Nationwide distribution including in the states of MD and MI. The countries of Austria, Belgium, France, Germany, Netherlands, Norway, South Africa, Spain, Switzerland, and United Kingdom.

Description

When strain relief is lost at the stand side of the Stand MVS Trolley Cable, over time one or more electrical contacts could break due to pulling, twisting, or dropping of the connector. If this happens, live parts may be exposed (230 V) and/or the video signal can be lost.

Product
Philips Zenition 70, System code 718133 - Product Usage: The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the device.
Manufacturer(s)
Philips North America, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Philips North America, LLC recalls Philips Zenition 70, System code 718133 - Product Usage: The devices are used for radiological guidance and visualizatio | RecallWatchUSA