Every recall we track for Philips Electronics North America Corporation — 70 in all — plus the complaints and injury reports the public filed about them.
Philips recalls Xper Flex Cardio Physiomonitoring System software versions 1.5.16.0322 and 1.6.1.0390 with model numbers 453564241901 and others. These versions may display inaccurate waveforms, frozen oxygen saturation readings, and blood pressure updates.
Philips recalls IntelliVue MX40 patient monitors with specific model numbers due to potential speaker issues at high altitudes. Affected units may have inaudible audio above 4,500 feet in Monitor Mode, but no immediate action is required.
Philips recalls Allura Xper F010 cardiac imaging systems with potential for ceiling monitor to detach and fall, risking injury to patient and users. Affected units sold 2003-2011.
Philips recalls Allura Xper FD2O Biplane systems with specific model codes from 2003 to May 2011 due to risk of monitor detachment and potential injury to patients or users.
Philips recalls AIIuraXperFDlO monitors from 2003-2011 due to potential ceiling suspension detachment causing monitor falls and injury risks. Affected units may need repair or replacement.
Philips recalls INTEGRIS Allura 9 F FDXD systems with specific model codes from 2003 to May 2011 due to risk of monitor ceiling suspension detaching and falling, potentially injuring patients or users.
Philips recalls INTEGRIS Allura 15-12 (biplane) systems with specific model codes from 2003 to May 2011 due to risk of monitor ceiling suspension detaching and falling, potentially injuring patients or users.
Philips recalls AlluraXperFOlO/lO systems with System Code 722005 from 2003 to May 2011 due to potential monitor detachment causing injury risks.
Philips recalls HM2000/3000 monitors with ceiling suspension that may detach, causing monitor falls and injury risk. Affected units sold 2003-2011.
Philips recalls Allura Xper F020 Biplane DR Tables (2003-2011) with potential monitor detachment risk. Affected units may cause patient or user injury if monitor falls from ceiling suspension.
Philips recalls Allura Xper F020 DR Tables (System Code 722023) from 2003-2011 where the monitor ceiling suspension may detach, risking injury to patients and users. Affected units have specific model codes and were sold in cardiac imaging applications.
Philips recalls Cesar Powerpack-Visub V3000 systems with Monitor Ceiling Suspension from 2003-2011 due to risk of monitor detachment and falling, potentially causing injury.
Philips recalls Allura Xper F010 DR Tables (2003-2011) with faulty ceiling monitor suspension that may detach and fall, risking injury to patients and users.
Philips recalls Allura Xper F020 DR Tables with System Code 722015 from 2003 to May 2011 due to risk of monitor detachment and falling, potentially injuring patients or users.
Philips recalls INTEGRIS Allura 9 systems with specific model codes from 2003 to May 2011 due to risk of monitor detachment and injury to patients or users.
Philips recalls AlIura Xper F010 F monitors from 2003-2011 due to potential ceiling suspension detachment causing monitor falls. Affected units may cause injury to patients, users or bystanders.
Philips recalls Allura Xper FD2O Biplane systems with specific model codes from 2003 to May 2011 due to risk of monitor detachment causing injury to patients and users.
Philips recalls Allura Xper F010/10 DRTable models from 2003 to May 2011 due to risk of monitor detachment and falling, potentially injuring patients or users.
Philips recalls certain cardiac imaging monitors from 2003-2011 due to risk of ceiling suspension detaching and causing injury to patients or users.
Philips recalls INTEGRIS Allura 15-12 (mono) systems with specific model codes from 2003 to May 2011 due to risk of monitor ceiling suspension detaching and falling, potentially injuring patients or users.
Philips recalls Allura Xper FD2O systems from 2003 to May 2011 due to potential monitor detachment causing injury risks. Affected units may need repair or replacement.
Philips recalls INTEGRIS Allura 9 (biplane) systems with Monitor Ceiling Suspension that may detach, causing monitor falls and injury risk. Affected units sold 2003-2011.
Philips recalls Allura Xper FD2O imaging systems with specific model codes from 2003-2011 due to risk of monitor detachment causing injury. Affected units may need repair or replacement.
Philips recalls AIIura Xper F010 DR Tables with System Code 722022 from 2003-2011 due to risk of monitor detachment and falling, potentially injuring patients or users.
Philips recalls INTEGRIS SUITE systems with Monitor Ceiling Suspension that may detach, causing monitor falls and injury risks. Affected units sold 2003-2011.
Philips recalls H3000 cardiac imaging monitors with ceiling suspension that may detach, causing injury. Affected units sold 2003-2011; stop using if monitor falls.
Philips recalls Allura Xper FD1O C systems (2003-2011) due to potential monitor detachment causing injury. Affected users should contact Philips for details.
Philips recalls INTEGRIS CV systems with ceiling monitor suspension from 2003-2011 due to risk of monitor detachment and injury to patients or users.
Philips recalls certain cardiac imaging monitors from 2003-2011 that may detach and fall, risking injury. Affected units have System Code 722011. Stop using immediately if you own one.
Philips recalls SureSigns VS3 Vital Signs Monitors with lithium batteries that may overheat or ignite after exceeding 3 years or 300 charge cycles. The existing labeling does not clearly show how to check battery age or cycles for replacement.
Philips recalls SureSigns VS2 vital signs monitors with lithium batteries that may overheat or ignite after exceeding 3 years or 300 charge cycles. The device could cause injury or property damage if the battery fails.
Philips recalls SureSigns VS4 Vital Signs Monitors (863283-863286) due to lithium-ion batteries overheating or igniting after exceeding 3-year life expectancy. Affected healthcare devices may cause injury or property damage if batteries fail.
Philips recalls SureSigns VSV monitors with lithium-ion batteries that may overheat or ignite after exceeding 3 years or 300 charge cycles. Replace batteries as instructed to prevent fire or injury.
Philips recalls SureSigns VM 3/4/6/8 patient monitors with lithium batteries that may overheat or ignite after exceeding 3-year life expectancy. Replace batteries every 3 years or after 300 charge cycles to prevent fire or injury.
Philips recalls HeartStart MRx defibrillators (models M3535A and M3536A) due to potential charging failure that could interrupt therapy. Affected units sold in the US from 2018-2020.
Philips recalls IntelliVue MX40 Patient Monitors with specific software versions due to missing warning statements in instructions. Affected units were sold since March 2:2016. No action required but check your device model.
Philips recalls IntelliVue MX40 Patient Monitors with specific software versions due to missing warning statements in instructions. Affected units may not follow safety guidelines properly.
Philips recalls IntelliVue MX40 patient monitors with software versions B.05-B.06.5X (released March 2:2016) due to missing warning statements in instructions. Affected units have model 865350 and date codes >= US096.
Philips recalls IntelliVue MX40 Patient Monitors with specific software versions due to missing warning statements in instructions. Affected units were sold since March 2016. No immediate action required but check for missing warnings.
Philips recalls ACS-NT Model 78108 MRI scanners due to potential helium gas release in MRI rooms during magnet quench events. This could create safety hazards in medical facilities using the device.
Philips recalls T5 Model 78104 MRI scanners due to potential helium gas release during magnet quench, which could create unsafe conditions in medical facilities.
Philips recalls specific Intera 1.5T MRI models due to potential helium gas release during magnet quench, which could create hazardous conditions in the exam room.
Philips recalls Intera 1.0T MRI scanners (Stellar Model 781102, Pular Model 781103) due to potential helium gas release during magnet quench, which could cause safety hazards in MRI rooms.
Philips recalls Ingenia 1.5T CX MRI scanners (models 781261 & 781262) due to potential helium gas release in the magnet quench process, which could create hazardous conditions in the exam room.
Philips recalls specific MRI systems due to potential helium gas release during magnet quench, which could cause injury. Affected models include Multiva 16, Multiva 8, and Achieva 1.5T systems. Contact Philips for details.
Philips recalls Panorama 1.0T MRI scanners (Model 781250) due to potential helium gas release during magnet quench, which could create a risk in the examination room.
Philips recalls Intera 0.5T Standard MRI models 781101 for potential helium gas release during magnet quench, which could cause safety hazards in MRI rooms.
Philips recalls T10-NT MRI scanners (model 78107) due to potential helium gas release during magnet quench, posing a risk in medical facilities. Affected units may require inspection or repair.
Philips recalls 1.5T MRI conversion devices (Model 781260) due to potential helium gas release during magnet quench, which could create unsafe conditions in MRI rooms.
Philips recalls specific Multiva MRI systems due to potential helium gas release during magnet quench, which could cause injury. Affected models include 1.5T 8 R5, 16 R5, and 8ch R5 systems with model numbers 781072-781078.
Philips recalls T5-NT MRI scanners (Model 78104) due to potential helium gas release in MRI rooms during magnet quench, which could create hazardous conditions.
Philips recalls Allura Xper R8.x and UNIZ systems with FlexVision monitors due to potential screen freezing during long procedures, which may disrupt imaging. Affected units include specific model numbers and versions.
Philips recalls HeartStart XL+ Defibrillators made before Sept 2017 that need software update A.03 for operational safety. Update to prevent incomplete device readiness checks.
Philips recalls QCPR meters used with HeartStart devices due to risks of improper pad placement during CPR. Affected units include specific model numbers sold with HeartStart FR3 or MRx devices.
Philips recalls QCPR meters used with HeartStart FR3 defibrillators due to risks of improper pad placement during CPR. Affected models include 861444, 861332, and others. Correct placement is critical for effective CPR.
Philips recalls Allura Xper systems with Certeray X-ray Generators in 480V regions due to risk of overheating and reduced X-ray performance from early ADU5 failures.
Philips recalls Intellivue iX surveillance stations that may lose patient monitoring if restarted after January 1, 2018. Users should avoid restarting these stations in 2018 to prevent temporary loss of monitoring.
Philips recalls Allura Xper FD10 and FD10/10 X-ray systems from 2003-2017 with risk of monitor falling if set screws loosen. Learn affected models and safety steps.
Philips recalls ProGrade R1 digital X-ray detectors with weak WiFi connections that may cause images to fail transferring to the system, requiring re-takes. Affected units have specific serial numbers.
