10,000 results
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47ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAN·April 8, 2024
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·April 8, 2024
BD PYXIS¿ MEDSTATION¿ ES
FDA Adverse Event
Malfunction
·CAREFUSION 303, INC.·Product code BRY·May 14, 2026
UNK COMPREHENSIVE REVERSE HUMERAL STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·January 28, 2021
UNK COMPREHENSIVE REVERSE HUMERAL STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·February 2, 2021
BD PYXIS¿ ES SERVER
FDA Adverse Event
Malfunction
·CAREFUSION 303, INC.·Product code BRY·April 8, 2026
UNK COMPREHENSIVE REVERSE GLENOSPHERE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·January 28, 2021
UNKNOWN COMPREHENSIVE REVERSE HUMERAL STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·January 28, 2021
UNKNOWN VRS
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·January 28, 2021
VITEK® 2 AST-P580 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·November 21, 2018
VITEK® 2 AST -P654 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·November 30, 2018
VITEK® 2 AST -P654 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·November 30, 2018
VITEK® 2 AST -P654 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·November 30, 2018
VITEK® 2 AST -P654 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·November 30, 2018
VITEK®2 AST-P631 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·September 5, 2018
VITEK® 2 AST-P635 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·March 6, 2019
VITEK®2 AST-P631 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·February 1, 2019
VITEK® 2 AST-P635 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·January 9, 2019
VITEK® MS
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code PEX·November 9, 2016
VITEK MS PRIME
FDA Adverse Event
Malfunction
·BIOMÉRIEUX, SA·Product code QBN·November 10, 2022