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Name Date Date initiated Country Source
Recall of Device Recall Digital Fluoroscopic Imaging System 2008-06-24 United States USFDA
Recall of Device Recall Digital Fluoroscopic Imaging System 2008-06-24 United States USFDA
Recall of Device Recall Digital Fluoroscopic Imaging System 2008-06-24 United States USFDA
Recall of Device Recall Digital Fluoroscopic Imaging System 2008-06-24 United States USFDA
Recall of Device Recall Digital Fluoroscopic Imaging System 2008-06-24 United States USFDA
Recall of Device Recall Nebion HLX8 magnetic resonance 2008-06-25 United States USFDA
Recall of Device Recall Command Module 2008-07-22 United States USFDA
Recall of Device Recall GasChex sterilization indicators 2008-02-07 United States USFDA
Recall of Device Recall CottonLeung Biliary Stent 2008-07-02 United States USFDA
Recall of Device Recall CottonLeung Biliary Stent 2008-07-02 United States USFDA
Recall of Weck Hemoclip Plus Ligating Clips 2003-10-24 United States USFDA
Recall of Device Recall Ultraview Digital Telemetry Transmitter 2008-07-17 United States USFDA
Recall of Device Recall GEM 2753 Microvascular Anastomotic Coupler 2008-05-14 United States USFDA
Recall of Device Recall Philips HeartStarMRtX 2008-07-14 United States USFDA
Recall of Device Recall Stableloc (TM) External Fixation System 2008-07-09 United States USFDA
Recall of Device Recall Fabius Trio Gas machine 2008-07-07 United States USFDA
Recall of Device Recall Isotechnology, Isobalance System 2008-07-09 United States USFDA
Recall of Device Recall Coulter LH SlideMaker 2008-05-29 United States USFDA
Recall of Device Recall PLV100 Portable Lifecare Ventilator 2008-07-08 United States USFDA
Recall of Device Recall GENS SlideMaker 2008-05-29 United States USFDA
Recall of Device Recall Ultraview Digital Telemetry Transmitter 2008-07-18 United States USFDA
Recall of Device Recall Philips Healthcare Informatics iSite PACS 2008-07-03 United States USFDA
Recall of Device Recall KyphX Osteo Introducer System 2008-06-23 United States USFDA
Recall of Device Recall Zimmer Alumina Ceramic Femoral Head 2008-06-11 United States USFDA
Recall of Device Recall Zimmer Alumina Ceramic Femoral Head 2008-06-11 United States USFDA