International Medical Devices Database

Data Source

Country

Device Classification

Parent Company

Name	Date initiated	Country	Source
Recall of Device Recall Poly Stim II Nerve Stimulator for Stryker Pain Pump	2010-02-01	United States	USFDA
Recall of Device Recall Single shot needle	2010-02-01	United States	USFDA
Recall of Device Recall Single shot needle	2010-02-01	United States	USFDA
Recall of Device Recall Single shot needle	2010-02-01	United States	USFDA
Recall of Device Recall Single shot needle	2010-02-01	United States	USFDA
Recall of Device Recall Nova StatStrip Glucose Test Strips	2010-02-12	United States	USFDA
Recall of Device Recall Single shot needle	2010-02-01	United States	USFDA
Recall of Device Recall Tuohy Catheter Kit	2010-02-01	United States	USFDA
Recall of Device Recall Tuohy Catheter Kit	2010-02-01	United States	USFDA
Recall of Device Recall Tuohy Catheter Kit	2010-02-01	United States	USFDA
Recall of Device Recall Tuohy Catheter kit	2010-02-01	United States	USFDA
Recall of Device Recall Image Consultant (IC) Software	2010-02-05	United States	USFDA
Recall of Device Recall Tuohy Stimulation Catheter Kit	2010-02-01	United States	USFDA
Recall of Device Recall Tuohy Stimulation Catheter Kit	2010-02-01	United States	USFDA
Recall of Device Recall Stimulation Catheter Continuous Nerve Block Tray	2010-02-01	United States	USFDA
Recall of Device Recall Stimulation Catheter Continuous Nerve Block Tray	2010-02-01	United States	USFDA
Recall of Device Recall Stimulation Catheter Continuous Nerve Block Tray	2010-02-01	United States	USFDA
Recall of Device Recall Olympus Trocar Spikes	2010-02-08	United States	USFDA
Recall of Device Recall Bevel Single Shot Needle	2010-02-01	United States	USFDA
Recall of Device Recall Stimulation Catheter Continuous Nerve Block Tray	2010-02-01	United States	USFDA
Recall of Device Recall Single Shot Needle	2010-02-01	United States	USFDA
Recall of Device Recall Single shot needle	2010-02-01	United States	USFDA
Recall of Device Recall Single shot needle	2010-02-01	United States	USFDA
Recall of Device Recall Grafix Tendon Stripper	2010-01-29	United States	USFDA
Recall of Device Recall KING LT D Size 4, 100003 Oropharyngeal Airway	2009-12-15	United States	USFDA

About this database

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

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)