Philips Electronics North America Corporation recalls

160 recalls on record · latest: November 15, 2018

Official U.S. recall history for Philips Electronics North America Corporation, compiled from official government records.

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Philips Electronics North America Corporation recalls Xper Flex Cardio Physiomonitoring System, Software versions 1.5.16.0322 and 1.6.1.0390, Model Numbers 453564241901, 453…

November 15, 2018 · Medical device recalls Moderate risk There are 3 issues: 1) Under certain conditions, real time waveforms may not be…

Philips Electronics North America Corporation recalls IntelliVue MX40 Patient Monitor, Model Nos. 865350, 865351, 865352, 867146 - Product Usage: Indicated for use by health…

October 10, 2018 · Medical device recalls Moderate risk A problem has been detected in the Philips IntelliVue MX4O that, if it were to…

Philips Electronics North America Corporation recalls AIIuraXperFDlO/10, System Code 722011 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls INTEGRIS CV, System Code 722030 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applic…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Allura Xper FD1O C, System Code 722001 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Poly C- DMCP-Visub(H3000), System Code 72238 Vascular, cardiovascular and neurovascular imaging applications, Cardiac i…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls INTEGRIS SUITE, System Code 722199 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging app…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls AIIura Xper F010 DR Table, System Code 722022 Vascular, cardiovascular and neurovascular imaging applications, Cardiac…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Allura Xper FD2O, System Code 722006 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging a…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls INTEGRIS Allura 9 (biplane), System Code 722021 Vascular, cardiovascular and neurovascular imaging applications, Cardia…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Allura Xper FD2O, System Code 722012 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging a…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls INTEGRIS Allura 15-12 (mono), System Code 722043 Vascular, cardiovascular and neurovascular imaging applications, Cardi…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls NTEGRIS Allura 9 0 FDXD, System Code 722498 Vascular, cardiovascular and neurovascular imaging applications, Cardiac im…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Allura Xper F010/10 DRTable, System Code 722019 Vascular, cardiovascular and neurovascular imaging applications, Cardia…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Allura Xper FD2O Biplane, System Code 722013 Vascular, cardiovascular and neurovascular imaging applications, Cardiac i…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls AlIura Xper F010 F, System Code 722002 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Allura Xper F020 DR Table, System Code 722015 Vascular, cardiovascular and neurovascular imaging applications, Cardiac…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Allura Xper F010 DR Table, System Code 722014 Vascular, cardiovascular and neurovascular imaging applications, Cardiac…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Cesar Powerpack-Visub(V3000), System Code 72243 Vascular, cardiovascular and neurovascular imaging applications, Cardia…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Allura Xper F020 DR Table, System Code 722023 Vascular, cardiovascular and neurovascular imaging applications, Cardiac…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Allura Xper F020 Biplane DR Table, System Code 722020 Vascular, cardiovascular and neurovascular imaging applications,…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Cesar-DMCP-Visub(HM2000/3000), System Code 72239 Vascular, cardiovascular and neurovascular imaging applications, Cardi…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls AlluraXperFOlO/lO, System Code 722005 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls INTEGRIS Allura 15-12 (biplane), System Code 722044 Vascular, cardiovascular and neurovascular imaging applications, Ca…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls INTEGRIS Allura 9 F FDXD, System Code 722497 Vascular, cardiovascular and neurovascular imaging applications, Cardiac i…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls AIIuraXperFDlO, System Code 722010 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging app…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Allura Xper FD2O Biplane, System Code 722008 Vascular, cardiovascular and neurovascular imaging applications, Cardiac i…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips Electronics North America Corporation recalls Allura Xper F010, System Code 722003 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging a…

July 16, 2018 · Medical device recalls Moderate risk There is a potential for the Monitor Ceiling Suspension, which holds a large sc…

Philips SureSigns VM 3/4/6/8 Patient Monitors recalled over fire hazard

July 13, 2018 · Medical device recalls Moderate risk Philips has received several reports in which monitors with lithium ion batteri…

Philips SureSigns VSV recalled over fire hazard

July 13, 2018 · Medical device recalls Moderate risk Philips has received several reports in which monitors with lithium ion batteri…

Philips SureSigns VS4 Vital Signs Monitor recalled over fire hazard

July 13, 2018 · Medical device recalls Moderate risk Philips has received several reports in which monitors with lithium ion batteri…

Philips SureSigns VS2 monitor recalled over fire hazard

July 13, 2018 · Medical device recalls Moderate risk Philips has received several reports in which monitors with lithium ion batteri…

Philips SureSigns VS3 Vital Signs Monitor recalled over fire hazard

July 13, 2018 · Medical device recalls Moderate risk Philips has received several reports in which monitors with lithium ion batteri…

Philips Electronics North America Corporation recalls HeartStart MRx Monitor/Defibrillator, Model No. M3535A (861288), M3536A (861289) Product Automated external defibrillat…

May 3, 2018 · Medical device recalls Moderate risk The MRx monitor/defibrillators could fail to charge because the therapy printed…

Philips Electronics North America Corporation recalls IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865352

April 30, 2018 · Medical device recalls Moderate risk Five warning statements are missing from the instructions for use.

Philips Electronics North America Corporation recalls IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865350

April 30, 2018 · Medical device recalls Moderate risk Five warning statements are missing from the instructions for use.

Philips Electronics North America Corporation recalls IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 867146

April 30, 2018 · Medical device recalls Moderate risk Five warning statements are missing from the instructions for use.

Philips Electronics North America Corporation recalls IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865351

April 30, 2018 · Medical device recalls Moderate risk Five warning statements are missing from the instructions for use.

Philips Electronics North America Corporation recalls T5-NT, Model 78104 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spec…

March 16, 2018 · Medical device recalls Moderate risk Potential risk for helium gas inside the MR examination room during a magnet qu…

Philips Electronics North America Corporation recalls Multiva systems, 1) Multiva 1.5T 8 R5 Model 781072, 2) Multiva 1.5T 16 R5 Model 781073, 3) Multiva 1.5T 8ch R5 based Mo…

March 16, 2018 · Medical device recalls Moderate risk Potential risk for helium gas inside the MR examination room during a magnet qu…

Philips Electronics North America Corporation recalls Conversion SmarthPath to dStream for 1.5T, Model 781260 Product Usage: Indicated for use as a diagnostic device. It can…

March 16, 2018 · Medical device recalls Moderate risk Potential risk for helium gas inside the MR examination room during a magnet qu…

Philips Electronics North America Corporation recalls Achieva 1.5T: 1) Nova (Dual), Model 781173, 2) Achieva 1.5T Initial Systems Model 781178, 3) Achieva 1.5T Nova Model 78…

March 16, 2018 · Medical device recalls Moderate risk Potential risk for helium gas inside the MR examination room during a magnet qu…

Philips Electronics North America Corporation recalls T10-NT, Model 78107 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spe…

March 16, 2018 · Medical device recalls Moderate risk Potential risk for helium gas inside the MR examination room during a magnet qu…

Philips Electronics North America Corporation recalls Intera 0.5T Standard, Model 781101 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectio…

March 16, 2018 · Medical device recalls Moderate risk Potential risk for helium gas inside the MR examination room during a magnet qu…

Philips Electronics North America Corporation recalls Panorama 1.0T, Model 781250 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional ima…

March 16, 2018 · Medical device recalls Moderate risk Potential risk for helium gas inside the MR examination room during a magnet qu…

Philips Electronics North America Corporation recalls Multiva systems; 1) Magnets Multiva 16 Model 781487, 2) Magnets 8 Model 781488, 3) Magnet Achieva 1.5T, Model 781492, 4…

March 16, 2018 · Medical device recalls Moderate risk Potential risk for helium gas inside the MR examination room during a magnet qu…

Philips Electronics North America Corporation recalls Ingenia 1.5T CX, Models 781261 & 781262 Product Usage: Indicated for use as a diagnostic device. It can produce cross-s…

March 16, 2018 · Medical device recalls Moderate risk Potential risk for helium gas inside the MR examination room during a magnet qu…

Philips Electronics North America Corporation recalls Intera 1.0T; 1) Stellar Model 781102, 2) Pular Model 781103 Product Usage: Indicated for use as a diagnostic device. It…

March 16, 2018 · Medical device recalls Moderate risk Potential risk for helium gas inside the MR examination room during a magnet qu…

Philips Electronics North America Corporation recalls Intera 1.5T; 1) Intera 1.5T Omni/Stellar Model 781104, 2) Intera 1.5T Power/Pulsar Model 781105, 3) Intera 1.5T Master/…

March 16, 2018 · Medical device recalls Moderate risk Potential risk for helium gas inside the MR examination room during a magnet qu…

Philips Electronics North America Corporation recalls T5 Model 78104 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectros…

March 16, 2018 · Medical device recalls Moderate risk Potential risk for helium gas inside the MR examination room during a magnet qu…

Philips Electronics North America Corporation recalls ACS-NT, Model 78108 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spe…

March 16, 2018 · Medical device recalls Moderate risk Potential risk for helium gas inside the MR examination room during a magnet qu…

Philips Electronics North America Corporation recalls Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray…

March 14, 2018 · Medical device recalls Moderate risk After continuous operation for more than one and a half days, the image on the…

Philips Electronics North America Corporation recalls HeartStart XL+ Defibrillator/Monitor The HeartStart XL+ is intended for use in a hospital setting by qualified medical…

February 7, 2018 · Medical device recalls Update XL¿ device software to version A.03. This includes enhancements to the O…

Philips Electronics North America Corporation recalls Philips QCPR Meter - used with FR3 Product Usage: The Philips CPR meter is intended for use with the Philips HeartStart…

January 29, 2018 · Medical device recalls Moderate risk Inform users of correct placement of the disposable adhesive pad on the QCPR me…

Philips Electronics North America Corporation recalls Philips QCPR Meter - used with MRx Product Usage: The Philips CPR meter is intended for use with the Philips HeartStart…

January 29, 2018 · Medical device recalls Moderate risk Inform users of correct placement of the disposable adhesive pad on the QCPR me…

Philips Electronics North America product recalled over fire hazard

January 4, 2018 · Medical device recalls Moderate risk There is an increase in the failure rate of certain Anode Drive Units (ADU5) us…

Philips Electronics North America Corporation recalls Intellivue iX Information Center Software - All PIIC iX Surveillance stations including: 866023 IntelliVue Info Center…

January 3, 2018 · Medical device recalls Moderate risk Once a surveillance station is restarted on January 1, 2018 or later, the stati…

Philips Electronics North America Corporation recalls Allura Xper FD and and Xper FD ORT - Philips X-ray Systems Product Usage: The Allura Xper FD10 and Alllura Xper FD10/10…

December 20, 2017 · Medical device recalls Moderate risk Extra monitors, so called 7th or 8th monitor, mounted on the Monitor Ceiling Su…

Philips Electronics North America Corporation recalls digital x-ray detector ProGrade R1 - solid state X ray imager (flat panel/digital imager) As a part of a radiographic s…

December 11, 2017 · Medical device recalls Moderate risk It the WiFi connection between the SkyPlate detector and HP transfer point is w…

Philips Electronics North America Corporation recalls IntelliVue X3 Patient Monitor.

November 17, 2017 · Medical device recalls Moderate risk The NBP measurement of Intellivue X3 Patient Monitor shows intermittently only…

Philips Electronics North America Corporation recalls CombiDiagnost R90 Image-Intensified fluoroscopic x-ray system CombiDiagnost R90 is a multi-functional general R/F syste…

October 19, 2017 · Medical device recalls Moderate risk The tube adapter-plate green/yellow protective earthing (PE) wire was removed.…

Philips Network Firewall recalled over fire hazard

October 5, 2017 · Medical device recalls Moderate risk Firewall installed with Philips IntelliVue Information Center iX or Information…

Philips Electronics North America Corporation recalls Automated External Defibrillator - HeartStart MRx Monitor/Defibrillator

September 28, 2017 · Medical device recalls Moderate risk Philips MRx devices have an EtCO2 module that may contain contamination; this c…

Philips Electronics North America Corporation recalls Philips SureSigns VSi / SureSigns VS2+ vital signs monitor used in healthcare environments and transport within a facil…

September 20, 2017 · Medical device recalls Some SureSigns VSi, VS2+ products have the Date of Manufacture on its serial nu…

Philips Electronics North America Corporation recalls IntelliVue Multi Measurement Server, IntelliVue Multi Measurement Server SLCP, IntelliVue Multi Measurement Server X2,…

August 23, 2017 · Medical device recalls Moderate risk Distorted ST-Segment when using 12-Lead ECG Monitoring with Philips IntelliVue…

Philips Electronics North America Corporation recalls Azurion 3 M12, Azurion 3 M15, Allura R9 7 M12, Allura R9 M20, Azurion 7 M12, Azurion 7 M20 The Allura Xper series is in…

August 18, 2017 · Medical device recalls Moderate risk When using the downscale option with the Allura R9 system or Azurion R1.1 syste…

Philips Electronics North America Corporation recalls ECG Out Cable - Heartstart MRx M1783A/M5526A 12-pin Sync cables All units of Philips sync cables model M1783A and M5526…

July 17, 2017 · Medical device recalls Moderate risk Issue with ECG out cables. When a Philips monitor/defibrillator is receiving an…

Philips Electronics North America Corporation recalls Mobile Detector Holder - Stationary X-ray System (RF System). suitable for positioning the wireless portable detector f…

July 14, 2017 · Medical device recalls Moderate risk If the lock mechanism of the movable camp of the mobile detector holder is not…

Philips Electronics North America Corporation recalls Philips DuraDiagnost X-ray systems: DuraDiagnost (R1.0, Product Number 712210) DuraDiagnost (R2.0, Product Number 71221…

May 31, 2017 · Medical device recalls Moderate risk Tube arm assembly could fall down due to cracked welding joints

Philips Electronics North America Corporation recalls Philips DigitalDiagnost 3.1.x X-Ray System

May 11, 2017 · Medical device recalls Moderate risk During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have identif…

Philips Electronics North America Corporation recalls NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)

May 4, 2017 · Medical device recalls Moderate risk Manufacturing defect may cause localized heating, which may result in localized…

Allura Xper Release 8 recalled over fire hazard

March 22, 2017 · Medical device recalls Moderate risk Due to a leak in the detector cooling system, cooling liquid may leak outside t…

Philips Electronics North America product recalled over fire hazard

March 22, 2017 · Medical device recalls Moderate risk Due to a leak in the detector cooling system, cooling liquid may leak outside t…

UNIQ: UNIQ FD10 recalled over fire hazard

March 22, 2017 · Medical device recalls Moderate risk Due to a leak in the detector cooling system, cooling liquid may leak outside t…

Philips Electronics North America Corporation recalls Philips IntelliVue MX4O WLAN Patient Wearable Monitor Product: 865352 Exchange part (service numbers): 453564615311 TEL…

March 6, 2017 · Medical device recalls Moderate risk Philips lntelliVue MX4O WLAN Patient Wearable Monitor may not automatically swi…

Philips Electronics North America Corporation recalls Philips Healthcare Brilliance iCT X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to p…

January 18, 2017 · Medical device recalls Moderate risk During a bolus tracking procedure, no images were generated when the scan was c…

Philips Electronics North America Corporation recalls Philips Healthcare Ingenuity CT X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to pro…

January 18, 2017 · Medical device recalls Moderate risk During a bolus tracking procedure, no images were generated when the scan was c…

Philips Electronics North America Corporation recalls Philips Healthcare Ingenuity Core128 X-Ray, Tomography, Computed These computed tomography x-ray systems are intended t…

January 18, 2017 · Medical device recalls Moderate risk During a bolus tracking procedure, no images were generated when the scan was c…

Philips Electronics North America Corporation recalls Philips Healthcare Ingenuity Core X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to p…

January 18, 2017 · Medical device recalls Moderate risk During a bolus tracking procedure, no images were generated when the scan was c…

Philips Electronics North America Corporation recalls Philips Healthcare Brilliance 64 System, X-Ray, Tomography, Computed These computed tomography x-ray systems are intend…

January 18, 2017 · Medical device recalls Moderate risk During a bolus tracking procedure, no images were generated when the scan was c…

Philips Electronics North America Corporation recalls Philips Healthcare Brilliance iCT SP X-Ray, Tomography, Computed These computed tomography x-ray systems are intended t…

January 18, 2017 · Medical device recalls Moderate risk During a bolus tracking procedure, no images were generated when the scan was c…

Philips Electronics North America Corporation recalls Philips Efficia CMS200 Central Monitoring System; 863352 The Efficia CMS200 central monitoring system is intended for u…

January 17, 2017 · Medical device recalls Moderate risk The monitor may not alarm appropriately for a pediatric or neonatal patient.

Philips Electronics North America Corporation recalls Philips Cisco 3850 layer 3 switch, 865339 model WS-C3850-12S-E in use with IntelliVue Information Center iX or Classic…

December 27, 2016 · Medical device recalls Moderate risk May experience a loss of centralized monitoring.

Philips Electronics North America Corporation recalls Velara Generator with an old Firmware version used with the Philips Integris BH5000

December 9, 2016 · Medical device recalls Moderate risk System may lock up.

Philips Electronics North America Corporation recalls Velara Generator with an old Firmware version used with Philips Allura Xper Systems (Allura 15 & 12 (monoplane), Allura…

December 9, 2016 · Medical device recalls Moderate risk System may lock up.

Philips Electronics North America Corporation recalls Ingenia MR-OR; 781437, 781438 The MR-OR option is intended for allowing transfer of a neurosurgical patient from OR sui…

December 1, 2016 · Medical device recalls Moderate risk Possibility that a patient or user may be exposed to a very small level of touc…

Philips Electronics North America Corporation recalls Allura Xper FD20 R8.2 722028 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnos…

December 1, 2016 · Medical device recalls Moderate risk Due to a production error, screws were not tightened to specified torque. These…

Philips Electronics North America Corporation recalls Allura Xper FD10 722026 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic,…

December 1, 2016 · Medical device recalls Moderate risk Due to a production error, screws were not tightened to specified torque. These…

Philips Electronics North America Corporation recalls Allura Xper FD20/15 R8.2 722058 is intended for: Cardiovascular and vascular X-ray imaging applications, including diag…

December 1, 2016 · Medical device recalls Moderate risk Due to a production error, screws were not tightened to specified torque. These…

Philips Electronics North America Corporation recalls Allura Xper FD20 722012 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic,…

December 1, 2016 · Medical device recalls Moderate risk Due to a production error, screws were not tightened to specified torque. These…

Philips Electronics North America Corporation recalls Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 Smart-hopping (2.4GHz) Product Number: 865351 Worldwide Except…

September 19, 2016 · Medical device recalls Moderate risk Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting Disables…

Philips Electronics North America Corporation recalls Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 WMTS Smart-hopping (1.4GHz) Product Number: 865350 Exchange pa…

September 19, 2016 · Medical device recalls Moderate risk Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting Disables…

Philips Electronics North America Corporation recalls Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 802.11a/b/g Product Number: 865352 Exchange part: 453564262491…

September 19, 2016 · Medical device recalls Moderate risk Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting Disables…

Philips Electronics North America Corporation recalls HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A

August 26, 2016 · Medical device recalls Moderate risk The handle can separate from the MRx housing due to breakage of mounts on the r…

Philips Electronics North America Corporation recalls PCR Compano Basic Reader using 100-127V as mains voltage. Model numbers: 732027, 732028, and 732040. Radiological image…

August 12, 2016 · Medical device recalls Moderate risk A defect component of the Compano reader power supply can cause the power suppl…

Philips Electronics North America Corporation recalls IntelliVue Patient Monitor Product Usage: The monitors are indicated for use by health care professionals whenever ther…

July 26, 2016 · Medical device recalls Moderate risk If an affected Patient Monitor has been powered on continuously for several mon…

Philips Electronics North America Corporation recalls MultiDiagnost Eleva; x-ray system. Product Codes: 708032, 708036

July 19, 2016 · Medical device recalls Moderate risk The two bolts that attach the clamping plate to the lateral shaft may break, wh…

Philips Electronics North America Corporation recalls UroDiagnost; x-ray system. Product Code: 708033

July 19, 2016 · Medical device recalls Moderate risk The two bolts that attach the clamping plate to the lateral shaft may break, wh…

Philips Electronics North America Corporation recalls MultiDiagnost Eleva with Flat Detector; x-ray system. Product Codes: 708034, 708037, 708038.

July 19, 2016 · Medical device recalls Moderate risk The two bolts that attach the clamping plate to the lateral shaft may break, wh…