764 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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GENVISC 850
FDA Adverse Event
Injury
·TEDEC-MEIJI FARMA·Product code MOZ·January 19, 2017
GENVISC 850
FDA Adverse Event
Injury
·TEDEC-MEIJI FARMA·Product code MOZ·January 24, 2017
GENVISC 850
FDA Adverse Event
Injury
·TEDEC-MEIJI FARMA·Product code MOZ·January 19, 2017
PCA KNEE
FDA Adverse Event
Injury
·HOWMEDICA, INC.·Product code JWH·September 25, 1995
2GX
FDA Adverse Event
Injury
·TISPORT, LLC·Product code IOR·June 27, 2019
2GX
FDA Adverse Event
Injury
·TISPORT, LLC·Product code IOR·August 16, 2018
2GX
FDA Adverse Event
Injury
·TISPORT, LLC·Product code IOR·January 10, 2019
TILITE 2GX
FDA Adverse Event
Injury
·TISPORT, LLC·Product code IOR·November 30, 2021
DUODOPA_DUOPA
FDA Adverse Event
Injury
·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·April 21, 2021
DUODOPA_DUOPA
FDA Adverse Event
Injury
·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·December 9, 2024
SEPRAFILM
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code MCN·April 3, 2023
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·UNKNOWN MANUFACTURING FACILITY·Product code KDJ·August 10, 2010
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·November 20, 2010
NI
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·November 21, 2017
BAIN FISTULA NEEDLE 1 5GX I, FIXED
FDA Adverse Event
Injury
·BAIN MEDICAL EQUIPMENT·Product code FIE·August 12, 2023
PRISMAFLEX SETS (ST)
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code KDI·October 20, 2022
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·UNKNOWN MANUFACTURING FACILITY·Product code KDJ·August 13, 2010
VITOSS BONE MARROW NEEDLES FENESTRATED 8G X 6
FDA Adverse Event
Injury
·STRYKER ORTHOBIOLOGICS-MALVERN·Product code KNW·February 19, 2016
PVP MEDIUM 6.4CM X 6.4CM
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·April 23, 2024
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·March 11, 2011