International Medical Devices Database

Data Source

Country

Device Classification

Parent Company

Name	Manufacturer	Risk Class	Country	Source
Device Recall PKG, BIPOLAR FORCEPS, MICRO TIP	Stryker Endoscopy	2	United States	USFDA
Device Recall PKG, METZENBAUM SCISSORS, STRAIGHT	Stryker Endoscopy	2	United States	USFDA
Device Recall PKG, ROTATING HANDLE, W/RATCHET, INSULATED SHAFT	Stryker Endoscopy	2	United States	USFDA
Device Recall PKG, OBTURATOR, 11MM, FOR HASSON CANNULA,	Stryker Endoscopy	2	United States	USFDA
Device Recall PKG, 5MM INSERT, BOWEL GRASPER FORCEPS, 45CM,	Stryker Endoscopy	2	United States	USFDA
Device Recall PKG, 3.5MM CANNULA AUTO VALVE, STOPCOCK, SHORT,	Stryker Endoscopy	2	United States	USFDA
Device Recall PKG, 3.5MM TROCAR, PYRAMIDAL TIP, SHORT,	Stryker Endoscopy	2	United States	USFDA
Device Recall PKG, 5MM INSERT, RETENTION GRASPER, 33CM	Stryker Endoscopy	2	United States	USFDA
Device Recall PKG, 5MM X 45CM INSERT, ALLIS FORCEPS, DOUBLE ROW TEETH,	Stryker Endoscopy	2	United States	USFDA
Device Recall GE Inspection Technologies Phoenix vtomex M240 cabinet xray systems.	GE Inspection Technologies, LP	Not Classified	United States	USFDA
Bard Orbiter PV Steerable Catheter \|\| Item #: 320100 (Marketed in Europe Only)	C. R.Bard, Inc./Electrophysiology Division		United States	USFDA
Device Recall Boston Scientific /Micorvasive	Boston Scientific Corporation		United States	USFDA
Amplicor [3] AV-HRP, Avidin-HRP (Horseradish Peroxidase) BGG Conjugate. \|\| Kit: AMPLICOR M. avium Detection Kit, Export,RUO.	Roche Molecular Systems Inc		United States	USFDA
VITEK 2 AST P612	Biomerieux Inc		United States	USFDA
VITEK 2 AST N190	Biomerieux Inc		United States	USFDA
VITEK 2 AST N230	Biomerieux Inc		United States	USFDA
VITEK 2 AST P625	Biomerieux Inc		United States	USFDA
VITEK 2 AST N330	Biomerieux Inc		United States	USFDA
Device Recall H. Pylori Ab Test CardSerum	LumiQuick Diagnostics Inc.		United States	USFDA
Device Recall Methamphetamine Strip	LumiQuick Diagnostics Inc.		United States	USFDA
Device Recall Propoxyphene Test Strip	LumiQuick Diagnostics Inc.		United States	USFDA
Device Recall Troponin I test Card (Whole Blood)	LumiQuick Diagnostics Inc.		United States	USFDA
Device Recall Matrix MAX 3	Skf USA Inc		United States	USFDA
Device Recall Matrix MAX 3	Skf USA Inc		United States	USFDA
Device Recall Epic II VR Model V158	St Jude Medical CRMD		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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