28 results · 29ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

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