10 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
UNK MAMMARY IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FWM·January 5, 2024
SYSTEM 9735542 15W VISUALASE
FDA Adverse Event
Death
·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code GEX·July 6, 2016
VISUALASE
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code GEX·May 15, 2019
GOOD SAM CINCINNATI OH 1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DWE·December 11, 2008
ARCHITECT TOTAL B-HCG REAGENT KIT
FDA Adverse Event
Malfunction
·A.I.D.D LONGFORD·Product code DHA·March 7, 2023
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013
TENDRIL DX
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011
LIFEPAK 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code LDD·March 13, 2008
INOVENT, NITRIC OXIDE DELIVERY SYSTEM
FDA Adverse Event
Injury
·MALLINCKRODT MANUFACTURING LLC.·Product code MRN·January 23, 2021
AU5400 CLINICAL CHEMISTRY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code JGS·January 7, 2014