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All product recalls associated with Philips Medical Systems.
Total Recalls
416
Past Year
97
Class I (Serious)
1
Most Recent
Oct 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Potential for erroneous measurements which may lead to incorrect diagnosis based upon the presence of an inaccurate, undetectable error in clinical measurement or calculation. If the user exits an imaging mode while Active Annotation is in use, the system can enter an undefined state where the image scale calibration may not match the scale of the on-screen measurements and graphics and possib
X-ray systems lack product report certification demonstrating compliance, and were illegally introduced into the United States commerce.
X-ray systems lack product report certification demonstrating compliance, and were illegally introduced into the United States commerce.