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  • Device 26490
  • Manufacturer 33665
  • Event 35826
  • Implant 7175
Name Date Date initiated Country Source
Recall of Device Recall Elecsys 2006-01-31 United States USFDA
Recall of Device Recall CryoValve 2006-01-27 United States USFDA
Recall of Device Recall CEDIA 2006-02-10 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of Device Recall Fem IM Nail 15mmdx48cm, Sterile, 2017-02-28 United States USFDA
Recall of Device Recall Fem IM Nail 16mmdx48cm, Sterile, 2017-02-28 United States USFDA
Recall of Device Recall Natus neoBLUE 2 Phototherapy system 2014-11-19 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of Device Recall INSTRUMENT ARM DRAPE, IS4000, 20 PACK 2015-06-16 United States USFDA
Recall of Device Recall OSSEOTITE Certain 2 Implant 2014-11-07 United States USFDA
Recall of Device Recall SOMATOM Spirit(Model 10045692 ) 2018-02-01 United States USFDA
Recall of Device Recall D240 (Lymphatic Marker) 2015-05-06 United States USFDA
Recall of Device Recall Cios Alpha 2015-05-05 United States USFDA
Recall of Device Recall BrainLAB Image Guided Surgery (IGS) System VectorVision fluoro 3D 2015-05-08 United States USFDA
Recall of Device Recall Intravascular Ultrasound System 2015-06-22 United States USFDA
Recall of Device Recall Intravascular Ultrasound System 2015-06-22 United States USFDA
Recall of Device Recall Smiths Medical 2014-11-21 United States USFDA
Recall of Device Recall Max Implant 2015-01-23 United States USFDA
Recall of Device Recall Intravascular Ultrasound System 2015-06-22 United States USFDA
Recall of Device Recall Fem IM Nail 15mmdx50cm, Sterile, 2017-02-28 United States USFDA
Recall of Device Recall Intravascular Ultrasound System 2015-06-22 United States USFDA
Recall of Device Recall STAIA PACK IRIInsulin 2018-03-05 United States USFDA
Recall of Device Recall 100/120V AC, Advanced Perfusion System Platform (APS) 2015-05-01 United States USFDA
Recall of Device Recall Brilliance CT Big Bore Oncology 2015-03-16 United States USFDA
Recall of Device Recall Brilliance CT 64 2015-03-16 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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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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