10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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TENEX TX2 PROCEDURE PACK
FDA Adverse Event
Injury
·TRICE MEDICAL·Product code LFL·September 25, 2025
TX SYSTEM - TX2 MICROTIP
FDA Adverse Event
Injury
·TENEX HEALTH, INC.·Product code LFL·March 31, 2026
BD SAFE-CLIP¿ NEEDLE CLIPPING DEVICE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·December 15, 2023
TENEX HEALTH TX SYSTEM - MICROTIP
FDA Adverse Event
Injury
·TENEX HEALTH·Product code LFL·September 11, 2017
TX2 TISSUE REMOVAL SYSTEM - MICROTIP
FDA Adverse Event
Malfunction
·TENEX HEALTH, INC.·Product code LFL·February 26, 2018
TX SYSTEM - TX2 MICROTIP
FDA Adverse Event
Injury
·TENEX HEALTH, INC.·Product code LFL·February 5, 2026
TOTAL ASR FEM IMP SIZE 53
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·March 13, 2013
TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code LOX·February 28, 2011
ACCU-CHEK ULTRAFLEX INFUSION SET
FDA Adverse Event
Injury
·DISETRONIC MEDICAL SYSTEMS·Product code FPA·February 21, 2008
AQUECOOL
FDA Adverse Event
Malfunction
·AQUEDUCT MEDICAL·Product code ILO·June 14, 2007