Medical Device Recall: Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System.
Philips North America Llc · March 10, 2025
Reason for Recall
Potential for collimator to fall as a result of incorrect installation.
Distribution
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.
States Affected
NATIONWIDE
Quantity Affected
83 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1553-2025
Status: ongoing
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