11 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
LONG NAIL KIT R1.5, TI, LEFT GAMMA3 10X260MM X 12
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 6, 2012
HUMERAL STEM 9MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·January 30, 2019
INSIGNIA
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·January 11, 2013
MINI-CAP, DISCONNECT W/PVP-1SOLUTION
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·November 30, 2010
HEARTSTART ONSITE
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·February 24, 2014
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·July 26, 2024
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·July 15, 2020
ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·December 6, 2024
HUMERAL STEM 9MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·February 18, 2010
UNIVERS HUMERAL HEAD 46/17
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·May 19, 2016
HUMERAL STEM 9MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·October 1, 2015