28 results
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29ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
3.5FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN MANUFACTURING SOLUTIONS SA·Product code FOS·September 9, 2014
1.9F ARGYLE SINGLE LUMEN PICC
FDA Adverse Event
Malfunction
·COVIDIEN·Product code LJS·September 18, 2014
3.5FR P.U.R. UMBIL CATH X10
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·June 3, 2014
2.5FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·May 29, 2014
3.5FR URETHANE UMBCATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·June 17, 2014
2.5FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·May 29, 2014
3.5FR P.U.R. UMBIL CATH X10
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·November 7, 2014
3.5FR P.U.R. UMBIL CATH X10
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·October 3, 2014
3.5 FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·July 28, 2014
DUAL LUMEN INSERTION TRAY
FDA Adverse Event
Malfunction
·COVIDIEN, COVIDIEN MANUFACTURING·Product code LJS·September 18, 2014
DUAL LUMEN INSERTION TRAY
FDA Adverse Event
Malfunction
·COVIDIEN, COVIDIEN MANUFACTURING·Product code LJS·September 18, 2014
3.5FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·August 22, 2014
3.5FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·October 20, 2014
3.5FR DUAL-LUMEN UVC CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·October 20, 2014
3.5FR P.U.R. UMBIL CATH X10
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·February 4, 2015
5.0FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·October 31, 2014
2.5 FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·July 28, 2014
3.5FR URETHANE UMB CATH
FDA Adverse Event
Malfunction
·COVIDIEN MANUFACTURING SOLUTIONS SA·Product code FOS·September 2, 2014
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·May 23, 2014
PENUMBRA ASPIRATION PUMP
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code BTA·March 15, 2010