14 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
AMPLATZER SEPTAL OCCLUDER
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code MLV·February 20, 2024
CARE ASSIST BED
FDA Adverse Event
Malfunction
·HILL-ROM PLUVIGNER·Product code FNL·June 27, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 12, 2011
INCEPTA
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 29, 2014
QDOT MICRO
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·May 27, 2026
CORTRAK ENTERAL ACCESS SYSTEM
FDA Adverse Event
Injury
·AVANOS MEDICAL INC.·Product code KNT·February 19, 2020
QDOT MICRO
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·April 28, 2026
QDOT MICRO
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·May 19, 2026
NGEN RF GENERATOR
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·December 16, 2025
NGEN RF GENERATOR, JAPAN
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code LPB·April 21, 2023
VIPERWIRE, ADVANCE
FDA Adverse Event
Malfunction
·CARDIOVASCULAR SYSTEMS INCORPORATED·Product code MCW·June 27, 2025
DIAMONDBACK 360 CORONARY ORBITAL ATHERECTOMY SYSTEM (VIPERWIRE)
FDA Adverse Event
Injury
·CARDIOVASCULAR SYSTEMS, INC. (ABBOTT)·Product code MCX·February 19, 2024
QDOT MICRO
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·March 6, 2026
QDOT MICRO
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·February 6, 2026