Philips Medical Systems Nederland B.V. Recalls

Recall history in this database

Classification mix: Class II: 180, Class I: 20.

Medical DeviceSep 6, 2023

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Wireless Foot Switch distributed with Philips Allura recall — FDA Z-2485-2023

Loss of availability of the wireless foot switch during procedures.

Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Medical DeviceAug 9, 2023

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Azurion 7 M20. X-ray Image guided Therapy System recall — FDA Z-2284-2023

The bolts supporting the FlexMove Carriage may become loose and/or break, and cracks may appear in the suspension rail of the FlexMove Carriage.

Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Medical DeviceAug 9, 2023

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Allura Xper FD10 and FD20 recall — FDA Z-2283-2023

The bolts supporting the FlexMove Carriage may become loose and/or break, and cracks may appear in the suspension rail of the FlexMove Carriage.

Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Medical DeviceJun 7, 2023

Philips Azurion System with software versions: R2.2.O, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 recall — FDA Z-1647-2023

Potential Loss of X-ray-When the full disk capacity is reached, X-Ray functionality will cease to be available there will be a sudden interruption of the procedure

Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Medical DeviceMay 11, 2022

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Azurion systems with software release R1.x recall — FDA Z-0886-2022

In the Azurion system, the user can add a new study to a patient by selecting the option Add Study . The Add Study dialogue box is then displayed where the Patient Type is selected to…

Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Medical DeviceFeb 23, 2022

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Zenition 50, Model #718096 recall — FDA Z-0647-2022

Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issue. If the wireless foot switch fails, there could be a delay or interruption of procedure if…

Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Medical DeviceFeb 23, 2022

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Veradius Unity, Model #718132 recall — FDA Z-0649-2022

Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issue. If the wireless foot switch fails, there could be a delay or interruption of procedure if…

Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Medical DeviceFeb 23, 2022

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Zenition 70, Model #718133 recall — FDA Z-0648-2022

Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issue. If the wireless foot switch fails, there could be a delay or interruption of procedure if…

Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Understanding this recall history

This page summarizes recall records in which the official source identifies Philips Medical Systems Nederland B.V. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.