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  • Device 26490
  • Manufacturer 33665
  • Event 35826
  • Implant 7175
Name Date Date initiated Country Source
Recall of Device Recall Brilliance 16 Computed Tomography Xray systems 2016-03-24 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of Device Recall Precision Blood Glucose Test Strips 2002-11-08 United States USFDA
Recall of Device Recall Optima 2002-11-26 United States USFDA
Recall of iVIEW DAB Detecion Kit. || Catalog Number 760-091 2003-05-07 United States USFDA
Recall of Device Recall MagNA Pure LC 2003-05-27 United States USFDA
Recall of Device Recall Neonatal Total Galactose Test Kit 2003-05-30 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of Device Recall Neonatal Total Galactose Test Kit 2003-05-30 United States USFDA
Recall of IMMAGE IgM Reagent || Part No.: 447610 2003-06-06 United States USFDA
Recall of Array Systems Calibrator 5 || Part No. 465250 2003-12-17 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of LDL Cholesterol Reagent (LDLD) || Part No. 969706 2003-02-10 United States USFDA
Recall of Device Recall CryoValve 2004-12-17 United States USFDA
Recall of Device Recall Brilliance CT 16 Power Computed Tomography Xray systems 2016-03-24 United States USFDA
Recall of Device Recall Ingenuity Core Computed Tomography Xray systems 2016-03-24 United States USFDA
Recall of Device Recall Bac T/ALERT 3D Control Module 2005-05-27 United States USFDA
Recall of Device Recall Bac T/ALERT 3D Combination Module 2005-05-27 United States USFDA
Recall of Device Recall Ingenuity Core 128 Computed Tomography Xray systems 2016-03-24 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of Device Recall Bac T/ALERT 3D 60 2005-05-27 United States USFDA
Recall of Radiomat Lightweight Cassettes 2005-01-26 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 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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