16 results · 36ms · Sources: EU EUDAMED, US FDA

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SEE H10

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013

RU NOVOSIBIRSK

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·October 16, 2013

ST JOSEPHS PHOENIX, AZ 1

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code DWF·July 31, 2009

RU NOVOSIBRIRSK

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·April 11, 2013

RU NOVOSIBIRSK

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DWF·October 16, 2013

CP87170 DE MUENCHEN

FDA Adverse Event
Death ·SORIN GROUP ITALIA·Product code DTZ·July 15, 2011

MBT CEM KEEL TIB TRAY SZ2.5

FDA Adverse Event
Injury ·DEPUY (IRELAND) 9616671·Product code NJL·April 2, 2013

ACCU-CHEK SPIRIT

FDA Adverse Event
Injury ·ROCHE INSULIN SYSTEMS, INC.·Product code LZG·March 16, 2011

GE OEC 9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS, INC·Product code JAA·April 17, 2008

CP87641 GB SOUTHAMPTON

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA·Product code DWE·March 22, 2010

FEMUR TRABECULAR METAL CRUCIATE RETAINING (CR) NARROW POROUS

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MBH·April 19, 2019

ARTICULAR SURFACE FIXED BEARING CRUCIATE RETAINING (CR) LEFT 10 MM HEIGHT

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MBH·April 19, 2019

PERSONA TM PEGGED POROUS TIBIAL COMPONENT

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code OIY·September 2, 2016

D 100 PH.I.S.I.O. NEWBORN HOLLOW FIBER MEMBRANE OXYGENATOR WITH RESERVOIR

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code DTZ·March 28, 2017

BABY CONTROL COSYCOT INFANT WARMER

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code FMT·June 6, 2013

WALL MOUNT INFANT WARMER

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code FMT·September 16, 2011