• About the database
  • How to use the database
  • Download the data
  • FAQ
  • Credits
List view Cards view
  • Device 26490
  • Manufacturer 33665
  • Event 35826
  • Implant 7175
Name Date Date initiated Country Source
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
Recall of Device Recall Brilliance CT 40 2015-03-16 United States USFDA
Recall of Device Recall Brilliance CT 16 Power 2015-03-16 United States USFDA
Recall of Device Recall Brilliance CT 16 Water 2015-03-16 United States USFDA
Recall of Device Recall Brilliance CT 16 Air 2015-03-16 United States USFDA
Recall of Device Recall Codman 3000 Series Refill Set 2015-03-05 United States USFDA
Recall of Device Recall ThermoFlo 1 HME 2015-02-19 United States USFDA
Recall of Device Recall Brilliance CT 10 Air 2015-03-16 United States USFDA
Recall of Device Recall Brilliance CT 6 Air 2015-03-16 United States USFDA
Recall of Device Recall Autoject E1 Fixed needle device 2014-11-24 United States USFDA
Recall of Device Recall COOK Stiffened Micropuncture Introducer Set 2002-11-25 United States USFDA
Recall of Device Recall Brilliance iCT 2015-03-16 United States USFDA
Recall of Device Recall Ingenuity CT 2015-03-16 United States USFDA
Recall of Device Recall Biograph 64R TruePoint w/ TrueV, Model Number 10097290 2015-07-14 United States USFDA
Recall of Device Recall Siemens MAGNETOM systems 2015-03-09 United States USFDA
Recall of Device Recall CareFusion Vital Signs LightWand Stylet 2015-03-13 United States USFDA
Recall of Device Recall CareFusion Vital Signs Introduction Pack 2015-03-13 United States USFDA
Recall of Device Recall Spacelabs Pediatric Flow Sensor Kit 2015-03-05 United States USFDA
  • 1
  • 2
  • 3
  • …
  • Next ›
  • Last »

About this database

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

  • FAQ
  • About the database
  • Contact us
  • Credits

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

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.

Download the data

The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

Download all (zipped)