31 results
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39ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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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