8 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
CAPSURE SP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·May 8, 2008
HEARTMATE GOGEAR SHOWER BAG
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·December 19, 2019
HEARTMATE SYSTEM MONITOR
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·January 2, 2020
BMT SPLINED KNEE STM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code OIY·July 27, 2023
HEARTMATE MOBILE POWER UNIT, NA
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·December 27, 2019
HEARTMATE MOBILE POWER UNIT, NA
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·December 27, 2019
CATHERA
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·July 17, 2024
RIST
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA·Product code QJP·February 18, 2026