13 results
·
40ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ISTENT INJECT W TRABECULAR MICRO-BYPASS SYSTEM
FDA Adverse Event
Malfunction
·GLAUKOS CORPORATION·Product code OGO·January 13, 2020
INTRAOCULAR PRESSURE LOWERING IMPLANT
FDA Adverse Event
Malfunction
·GLAUKOS CORPORATION·Product code OGO·January 29, 2020
RESOLUTE ONYX RX
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code NIQ·January 31, 2019
RESOLUTE INTEGRITY RX
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code NIQ·April 9, 2019
COBAS 8000 CORE UNIT
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·October 14, 2014
SERIES 7000 STANDARD TIBIA
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·July 13, 2011
COLLEAGUE VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 24, 2008
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·January 19, 2018
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·February 9, 2018
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·February 6, 2018
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·March 26, 2018
RESOLUTE ONYX RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·July 1, 2021
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·February 14, 2018