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Philips North America Recalls
530 recalls on record · April 5, 2017 to July 1, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia Ambition X, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia Ambition S, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia 3.0T CX, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia 3.0T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia 1.5T S, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia 1.5T CX, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia 1.5T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls GYROSCAN T5-NT, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls GYROSCAN T5, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls GYROSCAN T10-NT, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls GYROSCAN ACS-NT, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Evolution Upgrade 3.0T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Enterprise 1.5T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Achieva XR, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Achieva 3.0TX for PET, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Achieva 3.0T for PET, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Achieva 3.0T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Achieva 1.5T Initial, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Achieva 1.5T Conversion, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Achieva 1.5T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 17, 2024Medical DevicesFDA
Philips North America recalls PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from V4.5.1.41921 to V4.5.1.41989-Intend
Hazard: Patient tabletop moved out to the home position during scan initialization, may cause operator/bystander staying by the rear of the table to collide with the moved tabletop and be injured
April 3, 2024Medical DevicesFDA
Philips North America recalls CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X
Hazard: It was found that the Care Assist mobile application (version 4.1.1 and earlier) would not play custom ringtones when iOS device screens were locked with a passcode.
April 3, 2024Medical DevicesFDA
Philips North America recalls Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PIC iX Hardware) runni
Hazard: It was found that the Care Assist mobile application (version 4.1.1 and earlier) would not play custom ringtones when iOS device screens were locked with a passcode.
February 21, 2024Medical DevicesFDA
Philips North America recalls ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150
Hazard: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a previous patients radiography (RAD) images when starting the next patient scan while the previous patient image export is still processing. If the issue occurs, there is a potential for incorrect patient data to be displayed in the image. Issue 2: Detector Access point: Security vulnerability specific to the Wireless Portable Detector configuration items in Philips Support Connect (PSC). Due to this vulnerability it is possible, with physical access to the system and knowledge of specific settings, to modify and export data to removable media (example: USB)
February 21, 2024Medical DevicesFDA
Philips North America recalls ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref: (1)706100 (2)706110
Hazard: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a previous patient s radiography (RAD) images when starting the next patient scan while the previous patient image export is still processing. If the issue occurs, there is a potential for incorrect patient data to be displayed in the image. Issue 2: Detector Access point: Security vulnerability specific to the Wireless Portable Detector configuration items in Philips Support Connect (PSC). Due to this vulnerability it is possible, with physical access to the system and knowledge of specific settings, to modify and export data to removable media (example: USB)
February 14, 2024Medical DevicesFDA
Philips North America recalls Ingenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 989710008732), patient transportation syst
Hazard: Magnetic materials were used for the wheels of trolley. Wheels with magnetic material might be attracted to MRI systems if the wheels are in the magnetic field.
February 14, 2024Medical DevicesFDA
Philips North America recalls Ingenia Elition X (Product Number 781358) - HA FlexTrak II (Accessory Number 989710008732), patient transportation syste
Hazard: Magnetic materials were used for the wheels of trolley. Wheels with magnetic material might be attracted to MRI systems if the wheels are in the magnetic field.
February 14, 2024Medical DevicesFDA
Philips North America recalls Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
Hazard: Magnetic materials were used for the wheels of trolley. Wheels with magnetic material might be attracted to MRI systems if the wheels are in the magnetic field.
February 14, 2024Medical DevicesFDA
Philips North America recalls BrightView XCT, gamma camera for SPECT; Model Nos.: 6-digit format 882482; 12-digit format 453560462131 45356074
Hazard: Detector may unexpectedly fall due to a component failure. If the detector is positioned below center of gantry, there is a potential for abrasion, contusion, laceration, and/or fracture to the patient's lower limbs, as well as an interruption to normal system operation. If detector is positioned above center of gantry, there may be an interruption to normal system operation.
February 14, 2024Medical DevicesFDA
Philips North America recalls BrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478; 12-digit format 453560824741 4535608292
Hazard: Detector may unexpectedly fall due to a component failure. If the detector is positioned below center of gantry, there is a potential for abrasion, contusion, laceration, and/or fracture to the patient's lower limbs, as well as an interruption to normal system operation. If detector is positioned above center of gantry, there may be an interruption to normal system operation.