3 results
·
16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·March 2, 2023
ACCLAIM ENCORE 2.25
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·February 7, 2014
MINI MAGNA-FX CANNULATED SCREW
FDA Adverse Event
Malfunction
·ZIMMER, INC.·Product code HWC·November 2, 2012