55 results · 35ms · Sources: EU EUDAMED, US FDA

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ZIMMER NEXGEN ARTICUL

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JWH·May 1, 2017

VANGUARD PFR FEMORAL LT SM

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code KRR·May 17, 2018

IMPAX CV REPORTING

FDA Adverse Event
Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013

POLIGRIP

FDA Adverse Event
Other ·GLAXOSMITHKLINE·Product code KOL·February 16, 2011

LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·February 14, 2008

STERNALOCK BLU SYSTEM BLADE, STERNALOCK POWERDRIVER

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·May 22, 2018

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·April 5, 2017

RIBFIX BLU SYSTEM CROSS DRIVE BLADE, LONG

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019

RIBFIX BLU SYSTEM CROSS DRIVE BLADE, LONG

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019

RIBFIX BLU SYSTEM CROSS DRIVE BLADE, LONG

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·January 27, 2017

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·October 25, 2016

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·June 8, 2016

STAGE ONE SELECT HIP STEM CEMENT SPACER MOLD

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWY·June 11, 2018

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS LLC·Product code OYC·August 3, 2018

TRIATHLON PS X3 TIBIAL INSERT

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·December 8, 2016

STEMMED TIBIAL COMPONENT FIXED BEARING PRECOAT FOR CEMENTED USE ONLY SIZE 3

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JWH·May 9, 2017

PROTECTOR P50 MULTIPACK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·August 14, 2020

BD PHASEAL PROTECTOR (P50 MULTI)

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·July 30, 2020