8 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
2001145-MMJB STIM MODULE CABLE
FDA Adverse Event
Malfunction
·C.R. BARD, INC.·Product code DRQ·May 12, 2004
REVERSE SHOULDER SYSTEM HUMERAL REVERSE METAPHYSIS +9MM/0
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·October 19, 2021
BD MALE LL ADAPTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·July 17, 2024
PROTECTOR P50 MULTIPACK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code ONB·August 29, 2020
TECNIS EYHANCE IOL WITH TECNIS SIMPLICITYTM DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·AMO PUERTO RICO MFG. INC.·Product code HQL·May 6, 2025
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013
THE KOH COLPOTOMIZER SYSTEM
FDA Adverse Event
Malfunction
·COOPERSURGICAL - THE KOH COLPOTOMIZER SYSTEM·Product code HEW·February 7, 2011
CONTOUR TEST STRIPS (50)
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC·Product code NBW·February 15, 2008