16 results
·
61ms
·
Sources: EU EUDAMED, US FDA
AFFLOVEST
FDA Adverse Event
Injury
·TACTILE SYSTEMS TECHNOLOGY INC DBA TACTILE MEDICAL·Product code BYI·May 25, 2024
FLEXITOUCH PLUS SYSTEM
FDA Adverse Event
Injury
·TACTILE SYSTEMS TECHNOLOGY INC DBA TACTILE MEDICAL·Product code JOW·November 21, 2024
NIMBL PNEUMATIC COMPRESSION SYSTEM
FDA Adverse Event
Injury
·TACTILE MEDICAL TECHNOLOGY, INC.·Product code JOW·November 12, 2025
TRIPOLE 16C LAMITRODE LEAD
FDA Adverse Event
Injury
·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·May 21, 2008
BALLARD TURBO-CLEANING CLOSED SUCTION SYSTEM FOR ADULTS, DOUBLE SWIVEL ELBOW
FDA Adverse Event
Malfunction
·Product code BSY·May 25, 2021
BALLARD CLOSED SUCTION SYSTEMS FOR NEONATES/PEDIATRICS, ELBOW WITH CAPS
FDA Adverse Event
Malfunction
·AVANOS MEDICAL INC.·Product code BSY·March 2, 2023
DUROM US ACETABAR COMPONENT 48/42 H
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·July 21, 2010
DUROM US ACETABAR COMPONENT 48/42 H
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·July 21, 2010
CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH - LARGE
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code DYB·January 1, 2024
9617604-2007-00004
FDA Adverse Event
Injury
·Product code JOH·January 26, 2007
MO.MA ULTRA
FDA Adverse Event
Malfunction
·INVATEC SPA·Product code NTE·December 7, 2018
ILS 25MM, CURVED
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 10, 2019
TD TORQUE LINE CATHETER
FDA Adverse Event
Malfunction
·ICU MEDICAL, INC.·Product code DYG·July 18, 2013
Eurolink Europe Compliance Limited
Authorized representative
🇮🇪 Ireland·35 Manufacturers·252 Devices
BLAST Bandage, sterile.
FDA Recall
Terminated
·Tactical Medical Solutions, Inc.·Product code FQM·April 17, 2018
BLAST Bandage, sterile.
FDA Enforcement
Class II
·Terminated·Tactical Medical Solutions, Inc.·August 1, 2018