8 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD VACUTAINER® K3E 3.6MG PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·August 6, 2024
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SWINFORD·Product code KDI·September 24, 2015
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 19, 2014
ENTRAK 2500
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code LLZ·May 12, 2011
M2A-MAGNUM MODULAR HEAD SZ 44MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·June 15, 2012
25MM VERSA-DIAL TAPER ADAPTOR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·June 12, 2023
BEARING +3 MM RETENTIVE THICKNESS 36 MM DIAMETER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·June 8, 2023
COMP RVRS 25MM BSPLT HA+ADPTR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·June 12, 2023