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
2025 device recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 145–156 of 2,908 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-0848-2026
Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS)
Downstream Occlusion alarms may occur during procedures using low flow infusion rates when a check valve* is added to the Ivenix Administration Set.
Fresenius Kabi USA, LL…MADec 10, 2025
Class IIOngoingZ-0847-2026
Baxter Healthcare Corporation recalls Welch Allyn INF BAG
Replacement bladder kit for the Welch Allyn two-piece reusable blood pressure cuff may contain a Large Adult size bladder rather than a Thigh size bladder in the replacement kits.
Baxter Healthcare Corp…ILDec 10, 2025
Class IIOngoingZ-0818-2026
GET TESTED INTERNATIONAL AB recalls 8 in 1 STI Test Kit
Distribution without premarket approval/clearance.
GET TESTED INTERNATION…Dec 10, 2025