7 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD PLASTIPAK CONCENTRIC LUER LOCK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·June 19, 2019
MINICAP TRANSFER SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 30, 2014
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 2, 2013
LIFEPAK 1000 DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·November 12, 2010
4.5MM TI CORTEX SCREW SELF-TAPPING 38MM
FDA Adverse Event
Malfunction
·SYNTHES GRENCHEN·Product code HWC·March 25, 2015
TI DHS®/DCS® COMPRESSION SCREW 36MM
FDA Adverse Event
Injury
·SYNTHES GRENCHEN·Product code JDO·March 23, 2015
HARMONIC SCALPEL HAND PIECE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 26, 2024