13 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
2520274-2013-01424
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·March 13, 2013
CAPSURE SP
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 25, 2011
ELITE PASS SHUTTLE NEEDLE, BOX OF 5
FDA Adverse Event
Malfunction
·SMITH & NEPHEW INC., ENDOSCOPY DIVISION·Product code FMI·February 20, 2008
Z.S.G.M. CUTTER 3:1 RATIO ( CAUTION: SHARP )
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL, INC.·Product code FZW·February 6, 2023
MASK OXYGEN MED CONC W/7FT U-CONN-IT TBG
FDA Adverse Event
Malfunction
·CAREFUSION·Product code BYG·July 23, 2012
MASK OXYGEN MED CONC W/7FT U-CONN-IT TBG
FDA Adverse Event
Malfunction
·CAREFUSION·Product code BYG·July 23, 2012
ZIMMER SKIN GRAFT MESHER
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL, INC.·Product code FZW·February 6, 2023
UNKNOWN OXFORD TIBIAL COMPONENT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code HRY·March 11, 2020
LIGHTSHEER EC
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·August 28, 2012
OXFORD UNI FEMORAL SM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·April 27, 2021
BIOMET SPINE FUSION SYSTEM
FDA Adverse Event
Injury
·BIOMET SPINE - BROOMFIELD·Product code MAX·July 1, 2016
BIOMET SPINE FUSION SYSTEM
FDA Adverse Event
Injury
·BIOMET SPINE - BROOMFIELD·Product code MAX·July 1, 2016
HANDLE CEV669B DIA 5MM ANG BIPOLAR
FDA Adverse Event
Injury
·INTEGRA MICROFRANCE S.A.S.·Product code GEI·November 12, 2019