PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Recalls
29 recalls on record in the United States
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15 OR Table; System Code: 722059;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 5 M12; System Code: (1)722227, (2)722231;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020,
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10F; System Code: 722002;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/10; System Code: 722029;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)72202
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230,
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20 OR Table; System Code: 722039;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)72203
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15; System Code: 722058;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20; System Code: 722038;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234,
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Vue Motion V12. Product Number: 1017979.
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10C; System Code: 722001;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips AneurysmFlow. Model Number: 001015. AneurysmFlow
Potential safety issue involving the Mean Aneurysm Flow Amplitude (MAFA) ratio of AneurysmFlow (Interventional Tool). Philips has determined that the MAFA ratio does not provide reliable prognostic information regarding aneurysm occlusion following Flow Diverter Stent treatment, however despite being stated in the IUF, it is being relied on for making clinical decisions.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion. System Code Description (Model Number): Azu
Potential for the bolts and plastic parts of the Cable Hose Carriers that hold the cable hose to the monitor ceiling suspension may loosen and/or break over time due to the forces applied when the monitor is moved or rotated.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion system; System Code Description (Model Numbers): Azu
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion systems not configured with an optional auxi
Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control module.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Integris-Allura system; System Code Description (Model Numbe
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura system; System Code Description (Model Numbers): Allu
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.
View recall details →