10 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SURGICLIP III APPLIER
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FZP·February 13, 2023
SURGICLIP III
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FZP·February 13, 2023
GORE TIGRIS® VASCULAR STENT
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code NIP·October 11, 2016
UNKNOWN DEPUY INSERT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code HSH·December 9, 2008
INTERSTIM II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·August 31, 2011
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·August 1, 2013
PREMIUM SURGICLIP III
FDA Adverse Event
Malfunction
·US SURGICAL PUERTO RICO·Product code FZP·March 22, 2023
PREMIUM SURGICLIP III
FDA Adverse Event
Malfunction
·US SURGICAL PUERTO RICO·Product code FZP·March 22, 2023
PADPRO:AD;RTRANS EL/LW, 12X7
FDA Adverse Event
Injury
·KATECHO, INC.·Product code MKJ·October 7, 2022
GORE TIGRIS® VASCULAR STENT
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code NIP·September 6, 2016