Philips North America Llc
437 federal recalls on file, showing the 162 from the last 12 months. 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.
- 2025-10-08FDA-DeviceClass IICheck your Philips Allura Xper FD10 system
Certain Philips Allura Xper FD10 X-ray systems may have a BIOS battery that depletes faster than expected, preventing the system from starting up. The system will not display any warning before the battery runs out of power.
- 2025-10-08FDA-DeviceClass IIContact Philips about Allura Xper FD10C system failure
The BIOS battery in some Philips Allura Xper FD10C X-ray systems may run out of power faster than expected. When this happens, the system will not start up, and there are no warning messages to alert users before the battery fails.
- 2025-10-01FDA-DeviceClass IIPhilips CT systems labeled as the following: 1. CT 6000, Model Number: 728307.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- 2025-10-01FDA-DeviceClass IIPhilips CT systems labeled as the following: 1. Ingenuity CT Family Brazil, Model Number: 728325.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- 2025-10-01FDA-DeviceClass IIPhilips CT systems labeled as the following: 1. Ingenuity Core128 / Elite China, Model Number: 728324.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- 2025-10-01FDA-DeviceClass IIPhilips CT systems labeled as the following: 1. IQon Spectral CT, Model Number: 728332.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- 2025-10-01FDA-DeviceClass IIPhilips CT systems labeled as the following: 1. Ingenuity CT 728326, Model Number: 728321. 2. Ingenuity CT 728326, Model Number: 728323. 3. Ingenuity CT, Model Number: 728326.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- 2025-10-01FDA-DeviceClass IIPhilips CT systems labeled as the following: 1. Brilliance iCT SP, Model Number: 728311.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- 2025-10-01FDA-DeviceClass IIPhilips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- 2025-10-01FDA-DeviceClass IIPhilips CT systems labeled as the following: 1. Big Bore RT, Model Number: 728242. 2. Brilliance CT Big Bore Oncology, Model Number: 728243. 3. Brilliance CT Big Bore, Model Number: 728244.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- 2025-10-01FDA-DeviceClass IIPhilips CT systems labeled as the following: 1. Brilliance 16 Power, Model Number: 728240. 2. Brilliance CT 16 Slice, Model Number: 728246. 3. Brilliance CT 6 Slice, Model Number: 728256.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- 2025-10-01FDA-DeviceClass IIPhilips CT systems labeled as the following: 1. Brilliance CT 40 Channel, Model Number: 728235. 2. Brilliance CT 64 Channel, Model Number: 728231. 3. Ingenuity Flex, Model Number: 728317
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
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