International Medical Devices Database

Data Source

Country

Device Classification

Parent Company

Name	Date initiated	Country	Source
Recall of AEM DISPOSABLE ELECTRODES,MODEL ESO300 SERIES	2010-04-05	United States	USFDA
Recall of AEM DISPOSABLE ELECTRODES,MODEL ESO300 SERIES	2010-04-05	United States	USFDA
Recall of AEM DISPOSABLE ELECTRODES,MODEL ESO300 SERIES	2010-04-05	United States	USFDA
Recall of AEM DISPOSABLE ELECTRODES,MODEL ESO300 SERIES	2010-04-05	United States	USFDA
Recall of AEM DISPOSABLE ELECTRODES,MODEL ESO300 SERIES	2010-04-05	United States	USFDA
Recall of Biokit and SureVue HSV2 Rapid Test	2010-04-14	United States	USFDA
Recall of Spacelabs Medical Vital Signs Monitor, Model 91220	2010-04-14	United States	USFDA
Recall of Passport A.R. Knee Instrumentation Distal Guide Stand	2010-04-05	United States	USFDA
Recall of Shiley Disposable Cannula Low Pressure Cuffed Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Shiley Disposable Cannula Low Pressure Cuffed Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Shiley Disposable Cannula Low Pressure Cuffed Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Device Recall TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS	2013-07-16	United States	USFDA
Recall of Shiley Disposable Cannula Low Pressure Cuffed Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Shiley Fenestrated Low Pressure Cuffed Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Shiley Fenestrated Low Pressure Cuffed Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Shiley Fenestrated Low Pressure Cuffed Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Shiley Fenestrated Low Pressure Cuffed Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Shiley Disposable Cannula Fenestrated Low Pressure Cuffed Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Device Recall TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS	2013-07-16	United States	USFDA
Recall of Shiley Disposable Cannula Fenestrated Low Pressure Cuffed Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Shiley Disposable Cannula Fenestrated Low Pressure Cuffed Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Shiley Disposable Cannula Fenestrated Low Pressure Cuffed Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Shiley Percutaneous Dual Cannula Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Shiley Percutaneous Dual Cannula Tracheostomy Tube	2010-04-13	United States	USFDA
Recall of Shiley Fenestrated Low Pressure Cuffed Tracheostomy Tube with Evacuation Line	2010-04-13	United States	USFDA

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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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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.

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