257 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Recall
×
COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002
FDA Recall
Terminated
·AtriCure, Inc.·Product code OCL·January 22, 2019
COBRA FUSION 150 Ablation System, Catalog # (REF) 700-001S
FDA Recall
Terminated
·AtriCure, Inc.·Product code OCL·January 22, 2019
COBRA FUSION 150 Ablation System (International Only), Catalog # (REF) 700-001MI
FDA Recall
Terminated
·AtriCure, Inc.·Product code OCL·January 22, 2019
COBRA FUSION 150 Ablation System, Catalog # (REF) 700-001
FDA Recall
Terminated
·AtriCure, Inc.·Product code OCL·January 22, 2019
1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack
FDA Recall
Open, Classified
·American Contract Systems, Inc.·Product code OJH·March 22, 2022
1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray
FDA Recall
Open, Classified
·American Contract Systems, Inc.·Product code OJG·March 22, 2022
Intelli-C: Right side suspended Tabletop, REF: 03400000; Left side suspended Tabletop, REF: 03400010, used with the Intelli-C X-ray system
FDA Recall
Open, Classified
·NRT X-RAY A/S Birkegardsvej 16 Hasselager Denmark·Product code OWB·April 17, 2024
Hologic 3Dimensions/Selenia Dimensions Models: RM-SDM-00001-3D SDM-00001-2D SDM-00001-3D SDM-05000-3D3 SDM-05000-2DC SDM-00001-M3D SDM-05000-3DC SDM-SYS-6000-3D SDM-05000-2D3 SDA-SYS-3000-2D SDM-00001 SDM-SYS-9000-2D SDM-00001-M2D 3DM-SYS-STD 3DM-SYS-STD-NS SDM-05000-2AC SDM-05000-2A2 SDA-SYS-3000-3D SDA-SYS-3000-3D-UPS SDM-SYS-6000-3D-HTC SDM-05000-2D2 SDM-05000-3D2 SDM-SYS-6000-2D SDM-SYS-9000-3D
FDA Recall
Open, Classified
·Hologic, Inc.·Product code OTE·January 16, 2023
SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC, SDA-SYS-3000-3D, SDM-SYS-6000-2D, SDM-SYS-6000-3D, SDM-00001-2D, SDM-00001-3D, SDM-00001-M2D, SDM-00001-M3D, SDM-05000-2A2, SDM-05000-2A3, SDM-05000-2AC, SDM-05000-2D2, SDM-05000-2D3, SDM-05000-2DC, SDM-05000-3D2, SDM-05000-3D3, SDM-05000-3DC, SDM-SYS-9000-2D, SDM-SYS-9000-3D.
FDA Recall
Open, Classified
·Hologic, Inc·Product code MUE·April 8, 2026
GE OEC 9900 Elite ESP fluoroscopic x-ray system. GE Healthcare, Surgery, Salt Lake City, UT. The system is intended to provide an x-ray display of human anatomy.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·August 29, 2008
OEC 9800 Image Intensified fluoroscopic x-ray system (includes OEC 9800, OEC FluoroTrak 9800 Plus, OEC 9800 Plus, and OEC 9800MD Motorized C-arm System), GE Healthcare, Surgery, Salt Lake City, UT.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·April 15, 2008
GE OEC 9800 Fluoroscopic X-Ray System, GE Healthcare, Surgery, Salt Lake City, Utah. The intended use of this device is to perform mobile fluoroscopic examination of human anatomy.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·August 12, 2008
GE OEC 9600 C-arm Fluoroscopy System, GE Healthcare, Surgery, Salt Lake City, Utah.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·July 2, 2008
OEC 9900 Elite Image-intensified fluoroscopic x-ray system (includes OEC 9900 Elite Fluoroscopy System and 9900 EliteMD Motorized C-arm System), GE Healthcare, Surgery, Salt Lake City, UT.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·April 15, 2008
GE OEC 9900 Elite Fluoroscopic X-Ray System, GE Healthcare, Surgery, Salt Lake City, Utah. The intended use of this device is to perform mobile fluoroscopic examination of human anatomy.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·August 12, 2008
InstaTrak 3500 Navigation and Visualization System
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code LLZ·December 13, 2004
GE Healthcare OEC 9900 mobile fluoroscopic x-ray system
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·December 14, 2007
FluroTrak 9800 Plus Navigation and Visualization System
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·December 13, 2004
ENTrak Plus Navigation and Visualization System
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code LLZ·December 13, 2004
InstaTrak 3000 Navigation and Visualization System
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code LLZ·December 13, 2004