12 results
·
37ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
3.0MM HEX DRIVER
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·September 11, 2025
BHR
FDA Adverse Event
Injury
·SMITH & NEPHEW ORTHOPAEDICS, LTD.·Product code NXT·March 26, 2013
SM204 M-SERIES W/BIG WHEEL
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·March 10, 2011
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·March 31, 2008
MPACT ACETABULAR SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·July 14, 2025
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·VANTIVE US HEALTHCARE LLC·Product code KDJ·April 14, 2025
3.0MM DRILL BIT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HTW·December 21, 2020
GMK SPHERE TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·July 15, 2025
MEDTRONIC TRANSCATHETER VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·June 2, 2022
LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·June 25, 2025
10MM/125 DEG TI CANN TFNA 170MM - STERILE
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HSB·September 13, 2021
BOLT FOR FEMORAL NECK SYSTEM 80MM LENGTH-STERILE
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code KTT·March 6, 2023