31 results
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52ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PHOTODYNAMIC BONE STABILIZATION SYSTEM
FDA Adverse Event
Injury
·ILLUMINOSS MEDICAL, INC·Product code QAD·December 14, 2023
UNKNOWN VARIAX 2 VOLAR MEDIAL RIM DR PLATE, LONG
FDA Adverse Event
Injury
·STRYKER GMBH·Product code HRS·September 23, 2025
UNKNOWN INTACT CONSOLE
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY, LLC·Product code KNW·February 8, 2018
UNKNOWN INTACT HANDLE
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY, LLC·Product code KNW·February 8, 2018
UNKNOWN INTACT WAND
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY, LLC·Product code KNW·February 8, 2018
CORAIL2 STD SIZE 11
FDA Adverse Event
Injury
·DEPUY FRANCE SAS - 3003895575·Product code KWA·May 2, 2019
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·November 7, 2019
MESH - COMPOSIX
FDA Adverse Event
Death
·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·January 19, 2011
S-ROM*SLEEVE PRX ZTT, 18B-SML
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·December 4, 2019
PINN SECTOR W/GRIPTION 50MM
FDA Adverse Event
Injury
·Product code LPH·December 4, 2019
HEARTWARE VENTRICULAR ASSIST SYSTEM - DRIVELINE
FDA Adverse Event
Injury
·HEARTWARE, INC.·Product code DSQ·December 18, 2017
12/14 ARTICUL 44MM M SPEC+1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·February 16, 2023
HEARTWARE VENTRICULAR ASSIST SYSTEM-DRIVELINE
FDA Adverse Event
Injury
·HEARTWARE, INC.·Product code DSQ·July 6, 2018
AIGIS-R MEDIUM
FDA Adverse Event
Injury
·TYRX, INC.·Product code FTL·April 26, 2018
UPPER MODULE, COM1
FDA Adverse Event
Injury
·Product code OOK·April 15, 2020
ADAPTER SLEEVES 12/14 +2
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·May 2, 2019
ARTEFILL DERMAL FILLER
FDA Adverse Event
Injury
·SUNEVA MEDICAL, INC.·Product code LMH·February 26, 2020
ACTIV.A.C.¿ ION PROGRESS¿ REMOTE THERAPY MONITORING SYSTEM
FDA Adverse Event
Injury
·KINETIC CONCEPTS, INC.·Product code OMP·December 13, 2021
PINN LNR CON +4 NEUT 28IDX50OD
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code KWZ·November 7, 2016
TURBO-POWER LASER ATHERECTOMY CATHETER
FDA Adverse Event
Malfunction
·SPECTRANETICS CORPORATION·Product code MCW·March 8, 2024