439 results
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46ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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EVIS LUCERA ELITE BRONCHOVIDEOSCOPE
FDA Adverse Event
Injury
·AIZU OLYMPUS CO., LTD.·Product code EOQ·July 25, 2023
THORATEC® HEARTMATE 3® LVAS IMPLANT KIT
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·January 9, 2025
PREMILENE/MONOSYN SET
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL S.A.·Product code GAW·August 7, 2015
INOMAX DS (DELIVERY SYSTEM)
FDA Adverse Event
Injury
·INO THERAPEUTICS LLC.IKARIA·Product code MRN·November 16, 2011
INOMAX DE (DELIVERY SYSTEM)
FDA Adverse Event
Malfunction
·INO THERAPEUTICS LLC / IKARIA·Product code MRN·July 30, 2010
PINN MAR NEUT 28IDX46OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 21, 2020
SPYSCOPE DS II ACCESS & DELIVERY CATHETER
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code FBN·December 22, 2025
AMPLATZ SUPER STIFF
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·January 29, 2026
MICRA
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code PNJ·January 11, 2021
LUPINE BR DS W/ORTHCRD
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·April 1, 2024
FUKUDA DENSHI MODEL DS-5700 CENTRAL STATION
FDA Adverse Event
Malfunction
·FUKUDA DENSHI CO., LTD.·Product code DSI·December 15, 2004
NAVITOR VISION
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code NPT·June 27, 2025
CANDELA GENTLEMAX LASER SYSTEM
FDA Adverse Event
Malfunction
·CANDELA CORPORATION·Product code GEX·April 7, 2017
NAVITOR TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code NPT·April 16, 2026
FLEXNAV DELIVERY SYSTEM
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code NPT·October 31, 2025
FLEXNAV DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code NPT·September 16, 2025
INOMAX DS (DELIVERY SYSTEM)
FDA Adverse Event
Injury
·INO THERAPEUTICS LLC/ IKARIA·Product code MRN·December 20, 2011
IOLMASTER 500
FDA Adverse Event
Injury
·CARL ZEISS MEDITEC AG·Product code HJO·July 17, 2014
STOCKERT 70 RF GENERATOR
FDA Adverse Event
Injury
·STOCKERT GMBH·Product code DRF·December 28, 2011
SPECTRUM IQ
FDA Adverse Event
Malfunction
·BAXTER INTERNATIONAL INC.·Product code FRN·August 30, 2024