7 results
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29ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·January 9, 2013
TERUMO CDI 500 BLOOD PARAMETER MONITOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·December 6, 2010
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 18, 2014
JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023
JAWS "HIQ+", 5 X 330 MM, SCISSORS, METZENBAUM
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code HET·March 30, 2023
SHAFT "HIQ+", 5 X 330 MM
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code HET·May 23, 2023
JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023