27 results · 22ms · Sources: EU EUDAMED, US FDA

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S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 26, 2012

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 SENSOR MODULE FOR BUBBLE DETECTOR

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTW·October 21, 2016

GREENLIGHT MOXY FIBER OPTIC

FDA Adverse Event
Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·June 13, 2014

R3

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS, LTD.·Product code NXT·December 13, 2012

UNKNOWN DEPUY BONE CEMENT

FDA Adverse Event
Injury ·DEPUY CMW 9610921·Product code LOD·June 26, 2015

LCD TOUCHSCREEN, RP150, S5

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 14, 2012

LCD TOUCHSCREEN, RP150, S5

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 15, 2012

S5 SINGLE ROLLER PUMP

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·April 21, 2010

S5 ROLLER PUMP

FDA Adverse Event
Malfunction ·Product code DTQ·April 11, 2011

S5 SINGLE ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DWB·April 23, 2010

LCD TOUCHSCREEN, RP150, S5

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 16, 2012

S5 CONTROL PANEL MRP

FDA Adverse Event
Malfunction ·LIVANOVA DEUTSCHLAND·Product code DWB·July 18, 2018