Philips North America Llc
65 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Philips North America Llc and translate it into plain English — free weekly digest, optional same-day alerts.
- 2025-04-30FDA-DeviceClass IIVeradius Unity. Product Code 718132. 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 devices.
A wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.
- 2025-04-30FDA-DeviceClass IIZenition 70. Product Code 718133. 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 devices.
A wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.
- 2025-04-30FDA-DeviceClass IIZenition 50. Product Code 718096. 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 devices.
A wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.
- 2025-04-23FDA-DeviceClass IIPhilips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.
Potential for collimator to fall as a result of incorrect installation.
- 2025-04-23FDA-DeviceClass IIPhilips DXR System, DuraDiagnost 4.1. Stationary X-Ray System.
Potential for collimator to fall as a result of incorrect installation.
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