International Medical Devices Database

Data Source

Country

Device Classification

Parent Company

Name	Date initiated	Country	Source
Recall of LX125 Swivel Collimator, Model D800	2007-08-10	United States	USFDA
Recall of BARD Access Systems	2007-08-10	United States	USFDA
Recall of Ultrapower Bur	2007-08-09	United States	USFDA
Recall of BD Microkeratome K3000 and K4000	2007-08-09	United States	USFDA
Recall of LX125V Swivel Collimator, Model E600	2007-08-10	United States	USFDA
Recall of PCS125 Swivel Collimator, Model F100	2007-08-10	United States	USFDA
Recall of Merit Medical Surgical Convenience Kits	2007-08-15	United States	USFDA
Recall of Functional Anaesthetic Discography (F.A.D.) Catheter System	2006-04-25	United States	USFDA
Recall of Brain Heart Infusion Agar (BHIA)	2007-08-17	United States	USFDA
Recall of BardParker RibBack	2007-08-10	United States	USFDA
Recall of Multiple brand names including: Precision Xtra	2007-08-02	United States	USFDA
Recall of BardParker RibBack	2007-08-10	United States	USFDA
Recall of Pyrxis Anesthesia System 3500	2007-08-13	United States	USFDA
Recall of BHIA	2007-04-23	United States	USFDA
Recall of Coroskop Top XRay System	2008-08-11	United States	USFDA
Recall of Baxter Colleague CX Infusion Pumps	2007-08-15	United States	USFDA
Recall of Precision Implantable Pulse Generator	2007-08-03	United States	USFDA
Recall of MCT 100/480 ISOTRAN PLUS (AKA TEAL Power Conditioning Unit)	2007-04-27	United States	USFDA
Recall of Foundation Hip System Bipolar Modular	2007-08-02	United States	USFDA
Recall of PEMView	2007-08-01	United States	USFDA
Recall of Foundation Hip System Bipolar Modular	2007-08-02	United States	USFDA
Recall of Foundation Hip System Bipolar Modular	2007-08-02	United States	USFDA
Recall of Foundation Hip System Bipolar Modular	2007-08-02	United States	USFDA
Recall of Foundation Hip System Bipolar Modular	2007-08-02	United States	USFDA
Recall of Foundation Hip System Bipolar Modular	2007-08-02	United States	USFDA

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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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