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  • Device 1499
  • Manufacturer 316
  • Event 124969
  • Implant 36
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
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About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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