7 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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BARD® URETHRAL CATHETERIZATION TRAY WITH RED RUBBER CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·May 9, 2022
BARD® URETHRAL CATHETERIZATION TRAY WITH VINYL CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·May 9, 2022
BARD® URETHRAL CATHETERIZATION TRAY WITH VINYL CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·October 31, 2018
*
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INC.·Product code FAE·August 28, 2012
ACRYSOF
FDA Adverse Event
Malfunction
·ALCON MANUFACTURING, LTD.·Product code HQL·December 18, 2013
BASIS SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code KWP·July 23, 2010
LCP PROX-FEMPL 4.5/5 LE SHAFT 4HO L175 S
FDA Adverse Event
Malfunction
·SYNTHES ELMIRA·Product code HRS·June 25, 2013