99 results
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39ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
LO-PRO SCRW TM,SS 3.5X 14MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·June 2, 2020
LOCKING THIRD TUBULAR PLATE, SS, 10H
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·June 2, 2020
LO-PRO SCRW TM,SS 3.5X 14MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·June 2, 2020
LO-PRO SCRW TM,SS 3.5X 14MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·June 2, 2020
LO-PRO SCRW TM,SS 3.5X 18MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·June 2, 2020
LO-PRO SCRW TM,SS 3.5X 14MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·June 2, 2020
LO-PRO SCRW,SS 4.0X 14MMCANCLUS
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·June 2, 2020
LO-PRO SCRW TM,SS 3.5X 16MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·June 2, 2020
LO-PRO SCRW TM,SS 3.5X 18MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·June 2, 2020
CLAV FRAC PLT,CENTRAL THIRD,RT,SS
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·January 27, 2020
CLAV FRAC PLT,CENTRAL THIRD,LFT,SS
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·November 6, 2019
GRANUFLO
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 9, 2014
STANDARD POLYHESIVE II
FDA Adverse Event
Injury
·COVIDIEN VALLEYLAB·Product code GEI·October 19, 2010
NAIL
FDA Adverse Event
Injury
·SYNTHES USA·Product code JDS·December 21, 2012
LO-PRO SCRW TM,SS 3.5X 14MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·July 14, 2023
LO-PRO SCRW TM,SS 3.5X 14MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·August 21, 2019
LO-PRO SCRW TM,SS 3.5X 10MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·August 21, 2019
LO-PRO SCRW TM,SS 3.5X 12MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·August 21, 2019
COMPR FT SCRW,3.5 MINI,34MM LGTH
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·August 21, 2019
LO-PRO SCRW TM,SS 3.5X 40MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·August 21, 2019