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All product recalls associated with Philips Medical Systems North America Co. Phillips.
Total Recalls
1000
Past Year
272
Class I (Serious)
1
Most Recent
Dec 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.
Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.
A leak between the Tube Interface and the Outlet Tube of the transducer for the Respiratory Gating System component may result in a failure of the device to produce respiratory correlated images.
Potential for Internal Sound Amplifier to malfunction which could delay treatment.