7 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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LIBERTE MONORAIL CORONARY STENT DEL SYS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code MAF·October 27, 2006
UNI LFIT MEDIAL FEMORAL COMP.
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code HRY·April 15, 2013
LEVEL 1 HOTLINE LOW FLOW SYSTEMS
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code LGZ·January 23, 2024
LEVEL 1 HOTLINE LOW FLOW SYSTEMS
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code LGZ·January 23, 2024
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·January 11, 2013
ACCU-CHEK SPIRIT COMBO
FDA Adverse Event
Injury
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·November 24, 2010
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 3, 2014