Class IIOngoingZ-0857-2026
Philips North America LLC recalls IntelliVue MP80. Product Number: M8008A.
Potential issue where the IntelliVue monitors did not alarm.
Philips North America…MADec 10, 2025
Philips North America Llc recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 25–36 of 74 recalls
Class IIOngoingZ-0856-2026
Philips North America LLC recalls IntelliVue MP70. Product Number: M8007A.
Potential issue where the IntelliVue monitors did not alarm.
Philips North America…MADec 10, 2025
Class IIOngoingZ-0855-2026
Philips North America LLC recalls IntelliVue MP60. Product Number: M8005A.
Potential issue where the IntelliVue monitors did not alarm.
Philips North America…MADec 10, 2025
Class IIOngoingZ-0854-2026
Philips North America LLC recalls IntelliVue MP50. Product Number: M8004A.
Potential issue where the IntelliVue monitors did not alarm.
Philips North America…MADec 10, 2025
Class IIOngoingZ-0853-2026
Philips North America LLC recalls IntelliVue MP40. Product Number: M8003A.
Potential issue where the IntelliVue monitors did not alarm.
Philips North America…MADec 10, 2025
Class IIOngoingZ-0852-2026
Philips North America LLC recalls IntelliVue MP30. Product Number: M8002A.
Potential issue where the IntelliVue monitors did not alarm.
Philips North America…MADec 10, 2025
Class IIOngoingZ-0851-2026
Philips North America LLC recalls IntelliVue MP20. Product Number: M8001A.
Potential issue where the IntelliVue monitors did not alarm.
Philips North America…MADec 10, 2025
Class IIOngoingZ-0850-2026
Philips North America LLC recalls IntelliVue MP5. Product Number: M8105A.
Potential issue where the IntelliVue monitors did not alarm.
Philips North America…MADec 10, 2025
Class IIOngoingZ-0849-2026
Philips North America LLC recalls IntelliVue MP2. Product Number: M8102A.
Potential issue where the IntelliVue monitors did not alarm.
Philips North America…MADec 10, 2025
Class IIOngoingZ-2604-2025
Philips North America LLC recalls Philips CT systems labeled as the following: 1. CT 6000
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Philips North America…MAOct 1, 2025
Class IIOngoingZ-2603-2025
Philips North America LLC recalls Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Philips North America…MAOct 1, 2025
Class IIOngoingZ-2602-2025
Philips North America LLC recalls Philips CT systems labeled as the following: 1. Ingenuity Core128 / Elite China
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Philips North America…MAOct 1, 2025