110 results · 24ms · Sources: EU EUDAMED, US FDA

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SELECTRA MPH 55

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code DQY·August 17, 2018

SELECTRA MPH-45

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code DQY·October 20, 2016

SELECTRA MPH-45

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code DQY·February 7, 2018

SELECTRA MPH-45

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code DQY·April 26, 2018

SELECTRA MPH-45

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code DQY·August 28, 2017

TRACKMASTER

FDA Adverse Event
Malfunction ·JAS TRACKMASTER·Product code IOL·August 13, 2002

LOKOMAT

FDA Adverse Event
Malfunction ·REGULATORY INSIGHT, INC.·Product code IKK·March 22, 2016

SELECTRA MPH-45 GUIDING CATHETER

FDA Adverse Event
Malfunction ·BIOTRONIK·Product code DQY·August 24, 2017

TR-8500

FDA Adverse Event
Malfunction ·LIFE FITNESS, INC.·Product code IOL·May 21, 2004

QUINTON

FDA Adverse Event
Malfunction ·QUINTON INSTRUMENTS CO.·Product code IOL·July 1, 1997

EQUALIZER 6.0S

FDA Adverse Event
Malfunction ·PRO-FORM FITNESS PRODUCTS, INC.·Product code IOL·August 18, 1992

FREERIDER

FDA Adverse Event
Malfunction ·FREERIDER CORP·Product code INI·April 30, 2020

TREADMILL

FDA Adverse Event
Malfunction ·QUINTON INSTRUMENT CO.·Product code IOL·October 18, 1994

DIRECT PRESSURE MONITOR

FDA Adverse Event
Malfunction ·NEUROCARE GROUP, CAMINO·Product code GWM·January 25, 1999

FLEX-RUN WITH NIKE SOLE

FDA Adverse Event
Malfunction ·OSSUR HF·Product code ISH·December 22, 2020

IN X, FOR INLINE

FDA Adverse Event
Malfunction ·FERNO-WASHINGTON, INC.·Product code FPO·September 24, 2019

LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

FDA Adverse Event
Malfunction ·MEDTRONIC PHYSIO-CONTROL CORP.·Product code MKJ·April 4, 2001

TERADMILL T635M

FDA Adverse Event
Malfunction ·SPORTSART·Product code IOL·November 5, 2015

VMAX229 SERIES PULMONARY/METABOLIC SYSTEMS

FDA Adverse Event
Malfunction ·CAREFUSION·Product code BTY·October 28, 2015

ALTRUA 60

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC·Product code LWP·August 9, 2023