9 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
HUB SPIN-LOC THREADED LOCKING OEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FPA·April 9, 2021
ULTRA DRIVE 6MM PLUG PULLER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDX·July 20, 2022
BURRS
FDA Adverse Event
Malfunction
·MANSFIELD MANUFACTURING SITE·Product code HAB·March 20, 2013
INJECTOR, OPTIVANTAGE DH W/RFID
FDA Adverse Event
Injury
·LIEBEL-FLARSHEIM CO.·Product code IZQ·March 8, 2011
PULMONETIC
FDA Adverse Event
Malfunction
·CARDINAL HEALTH 203/PULMONETIC SYSTEMS, INC·Product code CBK·March 14, 2008
ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAT·March 9, 2022
PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code NEW·March 9, 2022
HUB SPIN-LOC THREADED LOCKING OEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FPA·March 19, 2021
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·August 15, 2017