9 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
VERTE-STACK K030736, K041197
FDA Adverse Event
Death
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code MQP·January 4, 2019
CORNERSTONE-SR CAGE SYSTEM
FDA Adverse Event
Death
·MSD DEGGENDORF MFG·Product code ODP·February 17, 2012
ZYDERM COLLAGEN IMPLANT
FDA Adverse Event
Injury
·COLLAGEN CORP.·Product code LMH·June 4, 1997
PUMP IN STYLE ADVANCED BREAST PUMP METRO BAG
FDA Adverse Event
Malfunction
·MEDELA, INC.·Product code HGX·March 21, 2013
SPRINT FIDELIS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 16, 2011
MONARCH III IOL DELIVERY SYSTEM CARTRIDGE - D
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code KYB·March 28, 2008
MEDTRONIC TRANSCATHETER VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·December 16, 2022
MEDTRONIC TRANSCATHETER VALVE
FDA Adverse Event
Death
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·December 16, 2022
BLOOD PUMP PU VALVES 30 ML, IN/OUT 9 MM
FDA Adverse Event
Malfunction
·BERLIN HEART GMBH·Product code DSQ·January 21, 2021