2,250 results · 31ms · Sources: EU EUDAMED, US FDA

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RADIOLOCENT DRIVE DRILL BIT

FDA Adverse Event
Malfunction ·STRYKER IRELAND LTD.·Product code GFF·July 12, 2011

BURR, OVAL, 8 FLUTE 4.0MM X 13CM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code GFF·October 4, 2018

4.5MM STERLING LIGHTNING BUR

FDA Adverse Event
Malfunction ·CONMED CORPORATION·Product code GFF·October 9, 2018

BURR, OVAL, 12 FLUTE 5.5MM X 13CM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code GFF·November 29, 2018

BUR,OVAL,FLUSHCUT,6 FLUT,5.MMX 13CM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code GFF·September 12, 2023

BURR, ROUND, 8 FLUTE 5.0MM X 13VM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code GFF·August 16, 2023

4.5MM X 19CM HPS PREBENT POLISHING BUR

FDA Adverse Event
Malfunction ·CONMED LARGO·Product code GFF·August 11, 2023

4.0MM ROUND SOLID CARBIDE BUR LONG

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code GFF·July 26, 2023

2.2MM LINDEMANN DRILL BIT

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code GFF·July 26, 2023

BUR,OVAL,FLUSHCUT,12 FLUT,5.0MMX 13CM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code GFF·August 11, 2023

BUR, SURGICAL, GENERAL AND PLASTIC SURGERY

FDA Adverse Event
Malfunction ·BRASSELER·Product code GFF·August 12, 2023

BUR,OVAL,CLEARCUT,8 FLUT,5.0MMX 13CM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code GFF·September 28, 2023

POWERASP,4.0MM X 13CM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code GFF·July 18, 2023

1.1MM DRILL BIT/MINI QC/45MM

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code GFF·September 12, 2023

POWERASP,4.0MM X 13CM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code GFF·August 4, 2023

BURR, OVAL, 8 FLUTE 5.0MM X 13CM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code GFF·September 18, 2023

2.2MM LINDEMANN DRILL BIT

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code GFF·October 28, 2025

BUR,RND,CLEARCUT,8 FLUT,5.5MMX 13CM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code GFF·October 7, 2025

BUR,RND,CLEARCUT,8 FLUT,5.5MMX 13CM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code GFF·October 7, 2025

BUR,RND,SJ,8 FLUT 3.0MMX 7CM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code GFF·September 22, 2025