Philips North America, LLC - Integris Allura 9 Interventional fluoroscopic xray system - Class 2 Recall
Integris Allura 9, system codes 722018 722021 (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 14, 2020 Category: Medical Devices Source Type: alerts
Philips North America, LLC - Integris Allura 15 & 12 Interventional fluoroscopic xray system - Class 2 Recall
Integris Allura 15 & 12, monoplane (system code 722043) and biplane (system code 722044) (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 14, 2020 Category: Medical Devices Source Type: alerts
Philips North America, LLC - Poly G Integris H5000 System, xray, angiographic - Class 2 Recall
Poly G Integris H5000, System code 72246 (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 14, 2020 Category: Medical Devices Source Type: alerts
Philips North America, LLC - Allura CV20 Interventional fluoroscopic xray system - Class 2 Recall
Allura CV20, system code 722031 (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 14, 2020 Category: Medical Devices Source Type: alerts
Philips North America, LLC - MultiDiagnost Eleva System, xray, angiographic - Class 2 Recall
MultiDiagnost Eleva, System codes 722030 722016 722017 708032 708036 708034 708037 708038 (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 14, 2020 Category: Medical Devices Source Type: alerts
Philips North America, LLC - UroDiagnost Eleva System, xray, angiographic - Class 2 Recall
UroDiagnost Eleva, system code 708033 (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 14, 2020 Category: Medical Devices Source Type: alerts
Philips North America, LLC - Cardio Vascular Allura Centron Interventional fluoroscopic xray system - Class 2 Recall
Cardio Vascular-Allura Centron, system code 722400 (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 14, 2020 Category: Medical Devices Source Type: alerts
Philips North America, LLC - Allura Xper FD Interventional fluoroscopic xray system - Class 2 Recall
Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 14, 2020 Category: Medical Devices Source Type: alerts
Philips Medical Systems Gmbh, DMC - CombiDiagnost PCF - Class 2 Recall
CombiDiagnost PCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, generalpurpose. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 21, 2020 Category: Medical Devices Source Type: alerts
Philips Medical Systems Gmbh, DMC - CombiDiagnostGCF - Class 2 Recall
CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, generalpurpose. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 21, 2020 Category: Medical Devices Source Type: alerts
Siemens Medical Solutions USA, Inc - ARTIS PhenoInterventional Fluoroscopic XRay System - Class 2 Recall
ARTIS Pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000 - Product Usage:AXIOM Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed with the AXIOM Artis family include cardiac angiography, neuro angiography, general angiography, rotational angiography, operating room angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures. Axiom Artis can also support the acquisition of position triggered imaging for...
Source: Medical Device Recalls - February 21, 2020 Category: Medical Devices Source Type: alerts
Siemens Medical Solutions USA, Inc - Uroskop Omnia max - Class 2 Recall
Uroskop Omnia max, Model No. 10762473 - Product Usage: Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an Xray pattern into a visible image. The system is designed primarily for urological diagnosis and the support of urological therapeutic applications such as examinations and small interventions of the urogenital tract. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 21, 2020 Category: Medical Devices Source Type: alerts
Carestream Health, Inc. - Kodak DirectView DR3000/3500 - Class 2 Recall
Kodak DirectView DR3000/3500 - Product Usage: permanently installed as a diagnostic system intended to generate and control x-rays for examination of various anatomical regions. The DR Operator Console is the user interface. All operator functions except positioning the Bucky assembly and controls for the collimator shutter are accomplished at the operator console. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 14, 2020 Category: Medical Devices Source Type: alerts
Hitachi Medical Systems America Inc - Hitachi Scenaria Wholebody Xray CT System - Class 2 Recall
Hitachi Scenaria Whole-body X-ray CT System (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 2, 2019 Category: Medical Devices Source Type: alerts
Deerfield Imaging, Inc. - IMRIS MR/Xray head fixation device - Class 2 Recall
IMRIS MR/X-ray head fixation device, Model HFD200 (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 19, 2019 Category: Medical Devices Source Type: alerts
