11 results
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40ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
GDC POWER SUPPLY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - FREMONT·Product code HCG·July 20, 2010
UNKNOWN PARIETEX PRODUCT
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code FTL·July 8, 2019
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 1, 2013
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC·Product code GJS·August 11, 2011
32MM -4 LFIT V40 HEAD
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·November 14, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2013
UNK SHOULDER GLENOID GLOBAL
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code HSD·July 25, 2022
UNKNOWN SCREW/ROD CONSTRUCT ACCESSORIES
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code MNH·January 3, 2020
UNKNOWN SCREW/ROD CONSTRUCT ACCESSORIES
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code MNH·January 6, 2020
UNKNOWN SCREW/ROD CONSTRUCT ACCESSORIES
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code MNH·January 6, 2020
COREVALVE TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·July 24, 2019