7 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SEE H10
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KXA·November 1, 2011
UNK
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code ORG·August 25, 2023
ZIMMER ELECTRIC DERMATOME HANDPIECE
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL·Product code GFD·February 27, 2013
PENUMBRA SYSTEM 054
FDA Adverse Event
Death
·PENUMBRA INC.·Product code NRY·February 15, 2011
COLLEAGUE VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·April 4, 2008
ACCESS® 2 IMMUNOASSAY CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHA·January 7, 2012
ANGEL CENTRIFUGE US (REFURBISHED)
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code ORG·August 24, 2023