26 results · 25ms · Sources: EU EUDAMED, US FDA

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TOSOH HLC-723GA ANALYZER G8

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·March 22, 2018

BD VACUTAINER® CD4 STABILIZATION BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·June 13, 2018

BD MULTITEST¿

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·July 5, 2023

TOSOH HLC-723G8 ANALYZER G8

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·March 14, 2018

AC*T DIFF 2

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·November 18, 2011

TOSOH HLC-723G8 ANALYZER G8

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·March 30, 2018

UNK - SCREWS: TRAUMA

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code HWC·January 9, 2023

TOSOH HLC-723G8 ANALYZER G8

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·April 2, 2018

TOSOH HLC-723G8 ANALYZER G8

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·May 22, 2018

STREAK

FDA Adverse Event
Injury ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code LOX·September 16, 1994

RX STREAK

FDA Adverse Event
Malfunction ·ACS·Product code GBA·July 29, 1994

3.0 RX STREAK

FDA Adverse Event
Malfunction ·ADVANCED CARDIOVASCULAR SYSTEM·Product code MJR·July 30, 1992

QUANTUM MAVERICK MONORAIL PTCA CATHETER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC·Product code LOX·January 4, 2006

TRECK CATHETER 4.0

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code LOX·November 12, 2014

NC TRECK 4.5

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code LOX·November 5, 2014

ACS RX STREAK 014

FDA Adverse Event
Death ·ADVANCED CARDIOVASCULAR SYSTEMS·Product code MFB·May 17, 1993

ACS RX STREAK 0.014

FDA Adverse Event
Injury ·ADVANCED CARDIOVASCULAR SYSTEMS·September 22, 1992

RX STREAK 0.14-2.25 BALLOON CATHETER

FDA Adverse Event
Malfunction ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code LOX·February 9, 1994

STREAK BALLOON CATHETER 3.0MM X 30 MM

FDA Adverse Event
Malfunction ·ADVANCED CARDIOVASCULAR SYSTEMS·Product code MFB·May 20, 1994

ACS RX STREAK .010 CATHETR DILATATION CATHETER

FDA Adverse Event
Injury ·ACS, INC.·Product code DSP·September 15, 1992