31 results · 39ms · Sources: EU EUDAMED, US FDA

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BAB TOUGH STRIPS WATERPROOF

FDA Adverse Event
Injury ·JOHNSON & JOHNSON CONSUMER INC·Product code KGX·August 26, 2021

ENDOKNOT PRE-TIED SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code MPN·December 4, 2023

THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER.

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code LPB·March 30, 2023

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·June 19, 2023

PROCEED*SURG MESH/MULTI LYR

FDA Adverse Event
Injury ·ETHICON INC.·Product code FTL·December 5, 2020

GORE® ACUSEAL VASCULAR GRAFT

FDA Adverse Event
Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·November 30, 2022

IMPRESS DIAGNOSITC PERIPHERAL CATHETER

FDA Adverse Event
Injury ·MERIT MEDICAL SYSTEMS, INC.·Product code DQO·May 13, 2015

SYNCHROMED EL

FDA Adverse Event
Injury ·RICE CREEK MANUFACTURING·Product code LKK·March 24, 2003

BIOMED

FDA Adverse Event
Injury ·BIOMET·Product code HSH·December 13, 2004

VENA TECH

FDA Adverse Event
Injury ·B. BRAUN MEDICAL, INC.·Product code DTK·December 9, 2002

6F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS

FDA Adverse Event
Injury ·ST. JUDE MEDICAL·Product code MGB·March 31, 2006

ACCU-CHEK ADVANTAGE

FDA Adverse Event
Injury ·ROCHE DIAGNOSITCS·Product code CFR·December 8, 2000

ACCU-CHEK COMFORT CURVE

FDA Adverse Event
Injury ·ROCHE DIAGNOSITCS·Product code LFR·September 17, 2002

ACCU-CHEK COMFORT CURVE

FDA Adverse Event
Injury ·ROCHE DIAGNOSITCS·Product code LFR·May 17, 2001

ACCU-CHEK COMFORT CURVE

FDA Adverse Event
Injury ·ROCHE DIAGNOSITCS·Product code CFR·September 17, 2001

OCTRODE LEAD KIT, 60CM LENGTH

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·August 28, 2015

VITROS HBSAG ASSAY

FDA Adverse Event
Injury ·ORTHO-CLINICAL DIAGNOSITCS·Product code LOM·February 25, 2009

CLOSER TSL6 FRENCH

FDA Adverse Event
Injury ·PERCLOSE, INC.·Product code MGB·August 30, 2000

6F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code MGB·September 2, 2004

ANGIO-SEAL

FDA Adverse Event
Injury ·QUINTON INSTRUMENT CO.·Product code MGB·April 30, 1998