11 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PULSE GEN MODEL UNK
FDA Adverse Event
Injury
·CYBERONICS·Product code LYJ·February 16, 2012
BIOGLUE SURGICAL ADHESIVE
FDA Adverse Event
Injury
·CRYOLIFE, INC.·Product code MUQ·December 1, 2010
CONSTELLATION VISIOIN SYSTEM
FDA Adverse Event
Malfunction
·ALCON-IRVINE TECHNOLOGY CENTER·Product code HQC·November 13, 2014
AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·UNKNOWN·Product code FNG·September 19, 2011
COULTER® LH 500 HEMATOLOGY INSTRUMENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·July 29, 2013
PULSE GEN MODEL UNKNOWN
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·February 16, 2012
PRODIGY AUTOCODE
FDA Adverse Event
Injury
·OK BIOTECH CO., LTD.·Product code NBW·May 9, 2017
UNKNOWN BONE CEMENT
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code LOD·December 10, 2019
UNKNOWN HIP FEMORAL STEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KXA·December 5, 2019
VERSAONE
FDA Adverse Event
Malfunction
·DAVIS & GECK CARIBE LTD·Product code GCJ·August 14, 2024
VERSAONE
FDA Adverse Event
Malfunction
·DAVIS & GECK CARIBE LTD·Product code GCJ·June 18, 2025