Every recall we track for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — 209 in all — plus the complaints and injury reports the public filed about them.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. is a leading manufacturer of medical imaging equipment and solutions.
PHILIPS
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. is a leading manufacturer of medical imaging systems and equipment. They provide a wide range of products including MRI, CT, X-ray, and ultrasound systems. Their products are used in hospitals and clinics worldwide for diagnostic imaging and patient care.
Philips recalls 15+ models of Allura Xper fluoroscopy systems due to potential loss of imaging functionality, motorized movement, or data from unauthorized hard drives. Affected units have specific model numbers listed in the recall.
Philips recalls Azurion 3 M12, M15, 5 M12, 5 M20, 7 B12, 7 B20, 7 M12, and 7 M20 X-ray systems with specific model numbers due to potential loss of imaging functionality from unauthorized hard drives.
Philips recalls specific models of interventional fluoroscopic X-ray systems (model 722400) due to unauthorized hard drives causing potential loss of imaging, movement, or data. Affected units have unique UDI numbers listed in the recall notice.
Philips recalls Allura Xper medical imaging systems with specific model numbers due to hand switch button not fully releasing, potentially causing loss of imaging or unintended radiation exposure.
Philips recalls specific MultiDiagnost Eleva models due to hand switch button not fully releasing, which may cause loss of imaging or unintended radiation exposure. Affected models include 708032-708038.
Philips recalls Allura Xper FD10 systems with HDDs that may degrade after 6 years, potentially causing imaging failures or motorized movement loss. Affected models include FD10, FD20 series with specific serial numbers.
Philips recalls Azurion 3 M12, M15, 5 M12, 5 M20, 7 B12, 7 B20, and 7 M12 models due to HDD performance degradation after 6 years of service, which may cause imaging or motorized movement failures. System restarts may temporarily restore function.
PHILIPS Medical Systems offers a wide range of medical imaging systems including CT, MRI, Ultrasound, and more. Our products are designed to provide high-quality imaging solutions for healthcare professionals.
Philips recalls specific Integris-Allura X-ray systems due to potential oil leakage in cooling units, which may cause system shutdowns. Affected models include Integris CV Cesar-Powerpack-Visub-Nicol (722030) and others manufactured between Feb 2016 and May 2020.
Philips recalls Azurion systems not configured with auxiliary pan handle due to mechanical wear in Float Tabletop control affecting table movements. Affected models include Azurion 3 M12, M15, 5 M12, 5 M20, 7 B12, B20, and 7 M12/M20 series with specific model numbers.
Philips recalls Azurion 3 M12, 3 M15, 7 B12, 7 B20, 7 M12 and 7 M20 models (2016-2020) due to potential oil leakage in X-ray tube cooling units that may cause system to switch to low-dose fluoroscopy. No remedy provided.
Philips recalls Azurion 3 M12, M15, 5, 5 M12, 5 M20, 7, 7 B12, 7 B20, 7 M12, 7 M20 models due to potential loosening/breaking of cable hose carriers bolts and plastic parts when monitor is moved or rotated.
Philips recalls AneurysmFlow software (model 001015) due to potential unreliable Mean Aneurysm Flow Amplitude (MAFA) ratio for aneurysm occlusion predictions. This could lead to incorrect clinical decisions during stent treatment.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
PHILIPS recalls ALLURA Xper FD10 X-ray systems with specific system codes (722003, 722010, 722026) due to potential failure to initiate X-ray imaging when using the wired foot switch.
Philips recalls Azurion 7 B12 X-ray systems with specific system codes due to potential failure to initiate X-ray imaging when using the wired foot switch.
Philips recalls Allura Xper FD10C X-ray systems with system code 722001 due to potential failure to initiate X-ray imaging when using the wired foot switch. Affected units may require repair to ensure safe operation.
Philips recalls Azurion 7 M20 X-ray systems with specific system codes (722079, 722224, 722234, 722282) for potential failure to initiate X-ray imaging when using the wired foot switch.
Philips recalls Xper FD20 X-ray systems with specific system codes due to potential failure to initiate X-ray imaging when using the wired foot switch. Affected units may not start or intermittently stop X-ray imaging during use. Consumers should contact Philips for details.
Philips recalls Allura Xper FD20/20 X-ray systems with System Code 722038 due to potential failure to initiate X-ray imaging when using the wired foot switch.
Philips recalls Allura Xper FD20/15 X-ray systems with specific system codes due to potential failure to initiate X-ray imaging when using the wired foot switch.
Philips recalls ALLURA Xper FD10 OR Table systems with specific serial numbers due to risk of improper X-ray imaging initiation. Affected units may require repair or replacement to ensure safe medical imaging.
Philips recalls X-ray imaging systems with specific serial numbers due to potential failure to initiate X-ray imaging when using the wired foot switch.
Philips recalls Allura Xper FD20/20 OR Table systems with System Code 722039 due to potential failure in initiating X-ray imaging when using the wired foot switch.
Philips recalls Azurion 7 M12 X-ray systems with specific system codes due to potential failure to initiate X-ray imaging when using wired foot switch. Affected units may require repair or replacement.
Philips recalls Azurion 3 M15 X-ray systems with specific system codes due to potential failure to initiate X-ray imaging when using the wired foot switch.
Philips recalls ALLURA Xper FD20 OR Table systems with specific system codes due to potential failure in initiating X-ray imaging when using the wired foot switch. Affected units may require repair or replacement.
Philips recalls Allura Xper FD20/10 X-ray systems with system code 722029 due to potential failure to initiate X-ray imaging when using the wired foot switch.
Philips recalls ALLURA Xper FD10F X-ray systems with system code 722002 due to potential failure to initiate X-ray imaging when using the wired foot switch.
Philips recalls ALLURA Xper FD20 Biplane or Table systems with specific serial numbers due to potential X-ray imaging failures when using the wired foot switch. Affected units may not initiate or intermittently produce X-rays, posing a risk of improper imaging during procedures.
Philips recalls Azurion 5 M12 X-ray systems with specific system codes due to potential failure to initiate X-ray imaging when using the wired foot switch. Affected units may require repair or replacement.
Philips recalls Azurion 7 B20 X-ray systems with specific system codes due to potential failure to initiate X-ray imaging when using the wired foot switch. Affected units may require repair or replacement.
Philips recalls Azurion 3 M12 X-ray systems with specific system codes due to potential failure to initiate X-ray imaging when using the wired foot switch.
Philips recalls Allura Xper FD20/15 OR Table systems with System Code 722059 due to potential failure to initiate X-ray imaging when using the wired foot switch.
Philips recalls ALLURA Xper FD20 Biplane systems with specific system codes due to potential failure to initiate X-ray imaging when using the wired foot switch.
Philips recalls Azurion 5 M20 systems with specific model numbers and software versions due to risk of unexpected table movement when pressing Reset Geometry button, even with lock engaged.
Philips recalls Azurion 7 B20 systems with specific model numbers and software versions due to risk of unexpected table movement when pressing Reset Geometry button, even with lock engaged.
Philips recalls Azurion 3 M12 systems with specific model numbers and software versions due to risk of unexpected table movement when pressing the Reset Geometry button, even with lock engaged.
Philips recalls Azurion 3 M15 systems with specific model numbers and software versions due to risk of unexpected table movement when pressing Reset Geometry button even with lock engaged.
Philips recalls Azurion 5 M12 systems with specific model numbers and software versions due to potential unexpected table movement when pressing Reset Geometry button, even with lock engaged.
Philips recalls Azurion 7 B12 systems with specific model numbers and software versions due to risk of unexpected table movement when pressing Reset Geometry button, even with lock engaged.
Philips recalls Azurion 7 M20 systems with specific model numbers and software versions due to risk of unexpected table movement when pressing Reset Geometry button, even with table lock engaged.
Philips recalls Azurion 7 M12 systems with specific model numbers and software versions due to risk of unexpected table movement when pressing Reset Geometry button, even with lock engaged.
Philips recalls limited Allura Xper FD20 systems (model 722006) where drip tray under cooling unit wasn't properly installed, risking coolant contact with electrical parts and system shutdown.
Philips recalls Allura Xper FD10 medical imaging systems with model 722026 where the drip tray under the cooling unit wasn't properly installed, risking electrical shorts and system shutdowns.
Philips recalls Allura Xper FD20 Biplane systems with model 722013 where drip tray under cooling unit may not be installed, risking electrical shorts and system shutdowns.
Philips recalls Allura Xper FD20 OR Table models with serial numbers 103, 10, 85, 125 due to potential coolant contact with electrical components if drip tray is not installed, risking system shutdown.
Philips recalls Allura Xper FD20 Biplane models with serial numbers starting with 296-488. If the drip tray under the cooling unit isn't installed, coolant could contact electrical parts, causing short circuits and system shutdowns.
Philips recalls Allura Xper FD10 medical imaging systems with model 722010 where drip tray under cooling unit wasn't properly installed, risking electrical shorts and system shutdowns.
Philips recalls Allura Xper FD20/10 systems with model 722029 where drip tray wasn't properly installed, risking electrical shorts and system shutdowns.
Philips recalls Allura Xper FD20 systems with model 722012 where the drip tray may not be installed, risking coolant contact with electrical parts and system shutdown.
Philips recalls Allura Xper FD10/10 systems with model 722005 due to potential coolant contact with electrical components if drip tray is not installed, risking system shutdown.
Philips recalls Allura Xper FD20/20 systems with model 722038 due to potential coolant contact with electrical components if drip tray is not installed, risking short circuits and system shutdowns.
Philips recalls Allura Xper FD10/10 systems with model 722011 where drip tray not installed may cause electrical short circuits and system shutdowns. Affected units have specific serial numbers.
Philips recalls Allura Xper FD10 medical imaging systems with model 722003 where the drip tray under the cooling unit wasn't properly installed. This could lead to coolant contacting electrical parts, causing short circuits and system shutdowns.
Philips recalls limited Allura Xper FD10C systems with model 722001 where drip tray under cooling unit wasn't properly installed. This could cause electrical shorts, system shutdowns, and potential safety risks.
