11 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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DIAMONDTEMP ABLATION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC·Product code OAE·August 9, 2023
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code LWS·April 10, 2013
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·May 8, 2008
INTERSTIM
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·January 3, 2013
UNKNOWN CATHETER
FDA Adverse Event
Injury
·MEDTRONIC DOMINICANA·Product code JXG·December 17, 2025
TACTICATH¿ CONTACT FORCE ABLATION CATHETER, SENSOR ENABLED¿
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code OAE·May 4, 2023
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·March 22, 2019
PROLENE HERNIA SYSTEM MESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·March 22, 2019
ONYX ANEURYSM
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code OBA·March 30, 2015
EVIS LUCERA SMALL INTESTINAL VIDEOSCOPE
FDA Adverse Event
Injury
·AIZU OLYMPUS CO., LTD.·Product code FDA·February 18, 2026
IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·March 25, 2021