International Medical Devices Database

Data Source

Country

Device Classification

Parent Company

Name	Date initiated	Country	Source
Recall of Device Recall Synchromed II	2004-05-11	United States	USFDA
Recall of Device Recall 8870 Software Application Card Version AAA 02	2004-08-24	United States	USFDA
Recall of Device Recall Medtronic SynchroMed EL	2006-06-06	United States	USFDA
Recall of 8731SC: Intrathecal Catheter	2008-04-14	United States	USFDA
Recall of 8709SC: Indura 1P	2008-04-14	United States	USFDA
Recall of 8596SC: Intrathecal Catheter Pump Segment Revision Kit	2008-04-14	United States	USFDA
Recall of 8578: Suturless Pump Connector Revision Kit	2008-04-14	United States	USFDA
Recall of SYNCHROMED II - PROGRAMMABLE PUMP	2008-06-18	Canada	HC
Recall of Device Recall Medtronic SynchroMed II Programmable Pump	2008-08-25	United States	USFDA
Recall of Device Recall Medtronic SynchroMed II Programmable Pump	2008-08-25	United States	USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump	2008-08-25	United States	USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump	2008-08-25	United States	USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump	2008-08-25	United States	USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump	2008-08-25	United States	USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump	2008-08-25	United States	USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump	2008-08-25	United States	USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump	2008-08-25	United States	USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Infusion Pump	2008-08-25	United States	USFDA
Recall of Device Recall N'Vision software Application Card	2009-03-23	United States	USFDA
Recall of Device Recall SYNCHROMED II PROGRAMMABLE DRUG INFUSION SYSTEM	2009-07-01	United States	USFDA
Recall of Device Recall Medtronic Sutureless Pump Connector Revision Kit	2009-08-27	United States	USFDA
Recall of Device Recall Medtronic Intrathecal Catheter Pump Segment Revision Kit	2009-08-27	United States	USFDA
Recall of Device Recall Medtronic Intrathecal Catheter	2009-08-27	United States	USFDA
Recall of Device Recall Medtronic Indura 1P Intrathecal Catheter	2009-08-27	United States	USFDA
Recall of Device Recall Medtronic SynchroMed EL implantable drug pump	2011-01-14	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.

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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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