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Philips Medical Systems Nederlands Recalls
79 recalls on record · May 9, 2018 to June 30, 2021 · Medical Devices
Recalls by year
18
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21
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 30, 2021Medical DevicesFDA
Philips Medical Systems Nederlands recalls Philips Allura Xper System: Interventional Fluoroscopic X-Ray System Product No.: 722026, 722027, 722028, 722029, 72203
Hazard: Certain low-voltage DC power supplies (DCPS) used in these products may be subject to an increased probability of failure. Failure of a DCPS may result in the sudden loss of imaging functionality or mechanical movement, depending on what subsystems the DCPS is powering.
August 7, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Azurion lnterventional Fluoroscopic X-ray System, with software version 1.2
Hazard: Philips has discovered through customer complaints and internal testing an intermittent electronic product defect in accordance with 21 CFR 1003.2(b)(1). When performing Cine runs, the Azurion's automatic exposure control software may set technique factors that result in radiation emissions too low to obtain useful diagnostic images.
May 8, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Ingenia Ambition S (781359), Ingenia Ambition X (781356) with Magnet Energization Device (MED), Philips MR systems a
Hazard: Magnet Energization Device (MED) can have a residual voltage on output terminal, may cause electrical shocks to personnel servicing the MED, MDD or connected cabling.
April 24, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Foot Switches used with the following systems: 722001 Allura Xper FD 10 C 722002 Allura Xper FD10 F 722003 Allura
Hazard: Additional units have been identified for previous recall Z-1280-2016 (RES 69339): If a Footswitch is frequently used on a non-flat surface or in the pedestal, the footswitch pedals may get bent. This might cause an intermittent or continuous inability of making live fluoroscopy images or exposures.
April 24, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product Codes: 708037, 708038 Product The All
Hazard: Additional units have been identified for previous recall Z-1280-2016 (RES 69339): If a Footswitch is frequently used on a non-flat surface or in the pedestal, the footswitch pedals may get bent. This might cause an intermittent or continuous inability of making live fluoroscopy images or exposures.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Multiva 1.5T, Model Number 781076. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Multiva 1.5T 8 R5, Model Number 781074. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls MARLIN 1.5T, Model Number 781474. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls NZM101 Ingenia 1.5T Linac, Model Number 781483. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Achieva 3.0T TX for PET, Model Number 781479. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Achieva 3.0T for PET, Model Number 781477. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls MR RT, Model Number 781439. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls MR-OR 3.0T, Model Number 781438. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls MR-OR 1.5T, Model Number 781437. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Ingenia Elition X, Model Number 781358. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Ingenia Elition S, Model Number 781357. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Ingenia Ambition X, Model Number 781356. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Ingenia Ambition S, Model Number 781359. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Ingenia 1.5T, Model Number 781396. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Ingenia 3.0T, Model Number 781377. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Panorama 1.0T, Model Number 781350. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Ingenia 1.5T S, Model Number 781347. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Achieva 1.5T Conversion, Model Number 781346. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Achieva 3.0T TX, Model Number 781345. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Achieva 3.0T X, Model Number 781344. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Achieva 1.5T, Model Number 781343. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Ingenia 3.0T, Model Number 781342. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Ingenia 1.5T, Model Number 781341. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Achieva 1.5T, Model Number 781296. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
March 6, 2019Medical DevicesFDA
Philips Medical Systems Nederlands recalls Intera 1.5T High Performance, Model Number 781295. Nuclear Magnetic Resonance Imaging System
Hazard: There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.