Philips Medical Systems Nederl recalls

Philips Medical Systems Nederl has 200 recalls on record with the FDA and USDA, the earliest in 2022 and the latest reported on 19 Aug 2026. 200 are still ongoing. 96 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls200since 2022
Last 12 months96reported
Class I2010% of total
Ongoing200latest 19 Aug 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 20 10%Class II 180 90%Class III 0 0%

Why philips medical systems nederl is recalled

By year

Ongoing philips medical systems nederl recalls

200 active

All philips medical systems nederl recalls, newest first

200 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIPhilips Azurion recalled by Philips Medical SystemsPhilips Medical Systems NederlPotency & Assay
DeviceCLASS IIAllura Xper FD recalled by Philips Medical SystemsPhilips Medical Systems NederlOtherNationwide
DeviceCLASS IIPhilips Allura, Cardio Vascular-Allura Centron recalledPhilips Medical Systems NederlOtherNationwide
DeviceCLASS IIPhilips Allura Xper with the following recalledPhilips Medical Systems NederlOther
DeviceCLASS IIPhilips MultiDiagnost Eleva with the following recalledPhilips Medical Systems NederlOther
DeviceCLASS IIPhilips Azurion 5M12 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIPhilips Azurion 7B20/15 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIPhilips Azurion 7M20 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIPhilips Azurion 5M20 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIPhilips Azurion 7M12 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIPhilips Azurion 7B12/12 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIPhilips Azurion 3M12 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIPhilips Azurion 3M15 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIIntegris-Allura system recalled by Philips Medical SystemsPhilips Medical Systems NederlPackaging DefectsNationwide
DeviceCLASS IIAzurion system recalled by Philips Medical SystemsPhilips Medical Systems NederlPackaging DefectsNationwide
DeviceCLASS IIPhilips Azurion recalled by Philips Medical SystemsPhilips Medical Systems NederlForeign MaterialNationwide
DeviceCLASS IIPhilips AneurysmFlow recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIAllura Xper; System recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIAzurion 7 B12 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIAllura Xper FD10C recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIVue Motion V12 recalled by Philips Medical SystemsPhilips Medical Systems NederlOtherNationwide
DeviceCLASS IIAzurion 7 M20 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIAllura Xper; System recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIAllura Xper FD20/20 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIAllura Xper FD20/15 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIAllura Xper OR Table recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIAllura Xper/10 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIAllura Xper FD20/20 OR Table recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIAzurion 5 M20 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide
DeviceCLASS IIAzurion 7 M12 recalled by Philips Medical SystemsPhilips Medical Systems NederlDevice MalfunctionNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.