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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.
May 29, 2024Medical DevicesFDA
Philips North America Llc recalls Achieva 3.0T Model Number (REF): (1) 781345; (2) 781344; (3) 781278; (4) 781277; (5) 781177
Hazard: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire
May 29, 2024Medical DevicesFDA
Philips North America Llc recalls Achieva 1.5T Initial system Model Number (REF): 781178
Hazard: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire
May 29, 2024Medical DevicesFDA
Philips North America Llc recalls Achieva 1.5T Conversion- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnosti
Hazard: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire
May 29, 2024Medical DevicesFDA
Philips North America Llc recalls Achieva 1.5T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device M
Hazard: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire
May 22, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia 3.0T with Evolution Upgrade 3.0T - - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated fo
Hazard: Philips Ingenia Evolution systems with software R5.7.1 may not provide warning for low ventilation setting which may lead to increase in body temperature or burning sensation
May 22, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia 1.5T with Evolution Upgrade 1.5T - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for
Hazard: Philips Ingenia Evolution systems with software R5.7.1 may not provide warning for low ventilation setting which may lead to increase in body temperature or burning sensation
May 22, 2024Medical DevicesFDA
Philips North America Llc recalls Patient Information Center iX and Patient Information Center iX Expand, Software Version 4.x.
Hazard: Event Catalog information does not save when copied and transferred from one unit to another.
May 8, 2024Medical DevicesFDA
Philips North America Llc recalls The Oncology Essentials Package of the Spectral CT imaging system.
Hazard: Potential for third party oncology marking laser to be reflected off the gantry cover surface, which can potentially lead to misdiagnosis and subsequent incorrect treatment.
May 1, 2024Medical DevicesFDA
Philips North America Llc recalls Philips Patient Information Center (PIC) iX Uninterruptable Power Supply (UPS): 1. APC (Schneider Electric IT Corporati
Hazard: Possible failure of Uninterruptable Power Supply (UPS) devices supporting the Patient Information Center (PIC) iX system, potential for the associated PIC iX system to shut down due to the lack of power. may lead to the delay in the detection of a change in a patient condition
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls SmartPath to dStream for XR and 3.0T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls SmartPath to dStream for 1.5T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls MR 7700, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls MR 5300, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera CV, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera Achieva 1.5T Pulsar, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 3.0T Quasar Dual, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T R11, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Power/Pulsar, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Omni/Stellar, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Master/Nova, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Explorer/Nova Dual, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Achieva Nova-Dual, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Achieva Nova, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Achieva IT Nova, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.0T Power/Pulsar, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.0T Omni/Stellar, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 0.5T Standard, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia Elition X, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia Elition S, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.