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Philips North America Llc recalls Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System.
Recalled April 23, 2025 · FDA recall Z-1553-2025 · Philips North America
Hazard
Potential for collimator to fall as a result of incorrect installation. · FDA Class II
Units
83 units
Sold at
Worldwide - US Nationwide distribution in the states of AK, FL, KS, MS, NH, NY, OR, PA, TX, WI and the countries of Argentina, Australia, Canada, Chile, China, Germany, Hungary, India, Indonesia, Italy, Kenya, Mexico, Netherlands, New Zealand, Oman, Pakistan, Peru, Poland, Romania, Russian Federation, Slovenia, South Africa, Spain, Thailand, United Kingdom, Vietnam.
Description
Potential for collimator to fall as a result of incorrect installation.
Product
Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System.
Manufacturer(s)
Philips North America Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →