13 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
REVERS LEVER-LOCKING BROACH HANDLE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·December 2, 2025
INTELLICUFF
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code BSK·January 13, 2024
INTELLICUFF
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code BSK·January 13, 2024
STANDARD C/D CLICKER MODEL
FDA Adverse Event
Injury
·ORTHOFIX SRL·Product code JDW·March 6, 2017
NAUTILUS REAMER/DRILL GLOVE PROTECTOR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·December 26, 2024
UNIVERS REVERS VERSION ROD
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·December 26, 2024
REVERS LEVER-LOCKING BROACH HANDLE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·November 17, 2023
REVERS LEVER-LOCKING BROACH HANDLE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·February 19, 2025
FREESTYLE LITE
FDA Adverse Event
Malfunction
·Product code NBW·February 8, 2013
INSIGNIA
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·January 6, 2011
WHITESTAR SIGNATURE SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL OPTICS·Product code HQC·July 22, 2014
UNIVERS REVERS VERSION ROD
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·November 27, 2024
REVERS LEVER-LOCKING BROACH HANDLE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·July 27, 2023