10,000 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code EZW·December 1, 2021
INTERLOCKING DETACHABLE COIL
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code KRD·August 24, 2011
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code EZW·August 10, 2021
VALLEYLAB ELECTROSURGICAL HANDSWITCHING PENCIL
FDA Adverse Event
Malfunction
·VALLEYLAB INC·Product code GEI·November 17, 1997
FIBERED IDC OCCLUSION SYSTEM
FDA Adverse Event
BOSTON SCIENTIFIC - CORK·Product code KRD·September 24, 2012
FIBERED IDC OCCLUSION SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - CORK·Product code KRD·June 9, 2011
RENEGADE STC 18 MICROCATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - CORK·Product code DQO·June 9, 2011
FIBERED IDC OCCLUSION SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code KRD·April 20, 2011
BARDEX® I.C. FOLEY CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code MJC·October 2, 2019
XPLORER 2200 DIGITAL RADIOGRAPHY SYSTEM
FDA Adverse Event
Malfunction
·IMAGING DYNAMICS COMPANY (IDC)·Product code KPR·March 21, 2012
XPLORER 2200 DIGITAL RADIOGRAPHY SYSTEM
FDA Adverse Event
Malfunction
·IMAGING DYNAMICS COMPANY (IDC)·Product code KPR·December 9, 2010
LIFE STAND
FDA Adverse Event
Injury
·IDC MEDICAL EQUIP. INC·Product code IOR·July 21, 1998
X3C 2200 WITH MAGELLAN 3.4 SOFTWARE INSATLLED
FDA Adverse Event
Malfunction
·IMAGING DYNAMICS COMPANY (IDC)·Product code KPR·July 30, 2009
INTERLOCK¿
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - CORK·Product code KRD·September 21, 2011
Rainbow DC-I-DC Pulse CO-Oximeter Sensor used with the Masimo SET Rad 57 Pulse CoOximeter
FDA Recall
Terminated
·Masimo Corporation·Product code DQA·February 2, 2006
INTERLOCK¿-35
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - CORK·Product code KRD·June 12, 2012
SFXSPI MCL+ BI UD 6IN2 3-0 DA RB-1
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·July 8, 2025
FIBERED IDC OCCLUSION SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code KRD·February 23, 2011
INTERLOCK¿-35
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code KRD·September 8, 2017
REZUM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·January 28, 2026