International Medical Devices Database

Data Source

Country

Device Classification

Parent Company

Name	Date	Date initiated	Country	Source
Field Safety Notices about SynchroMed EL implantable programmable pumps	2006-07-07		Germany	BAM
Field Safety Notices about SynchroMed® II			Slovenia	AMPMDRS
Field Safety Notices about SynchroMed® II			Slovenia	AMPMDRS
Field Safety Notices about SynchroMed® II Implantable Drug Infusion Pump			Slovenia	AMPMDRS
Field Safety Notices about SynchroMed® II Programmable Pump			Slovenia	AMPMDRS
Field Safety Notices about SynchroMed® II Implantable Infusion Pump			Slovenia	AMPMDRS
Safety Alert for SynchroMed Implantable Infusion Pump	2013-06-17		Hong Kong	DH
Safety Alert for SynchroMed II and SynchroMed EL pumps	2013-06-19		Hong Kong	DH
Safety Alert for SynchroMed II Implantable Drug Infusion Pump	2014-03-18		Hong Kong	DH
Safety Alert for SynchroMed II Implantable Drug Infusion Pump	2017-09-15		Hong Kong	DH
Safety Alert for SynchroMed Implantable Infusion Pump	2012-11-20		Hong Kong	DH
Safety Alert for 8870 Software Application Card used in the 8840 N’Vision Clinician Programmer	2013-10-10		Hong Kong	DH
Safety Alert for SynchroMed® II Pump	2012-03-20		Hong Kong	DH
Recall of Medtronic Implantable Programmable Infusion Pumps		2014-04-04	United States	USFDA
Recall of Medtronic SynchroMed II Implantable Infusion Pumps		2015-04-10	United States	USFDA
Recall of 8578: Suturless Pump Connector Revision Kit		2008-04-14	United States	USFDA
Recall of 8596SC: Intrathecal Catheter Pump Segment Revision Kit		2008-04-14	United States	USFDA
Recall of 8709SC: Indura 1P		2008-04-14	United States	USFDA
Recall of 8731SC: Intrathecal Catheter		2008-04-14	United States	USFDA
Recall of Device Recall Medtronic SynchroMed II		2011-07-05	United States	USFDA
Recall of Device Recall Medtronic, Model 8870, Application Software Card		2012-03-12	United States	USFDA
Recall of Device Recall SynchroMed EL implantable infusion pump		2012-11-09	United States	USFDA
Recall of Device Recall SynchroMed II implantable infusion pump		2012-11-09	United States	USFDA
Recall of Device Recall SynchroMed II Implantable Infusion Pump		2013-06-03	United States	USFDA
Recall of Device Recall SynchroMed II Implantable Infusion Pump		2013-06-03	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.