7 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OPTETRAK HI-FLEX TIBIAL INSERT SZ 5 15MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·July 17, 2024
CURRENT PLUS DR, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·November 10, 2014
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·July 22, 2013
THORATEC® HEARTMATE 3¿ VAD MODULAR CABLE
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·May 20, 2024
HLS SET ADVANCED 7.0
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·December 9, 2020
HEARTMATE 3 VAD MODULAR CABLE
FDA Adverse Event
Malfunction
·THORATEC CORPORATION·Product code DSQ·June 1, 2022