19 results
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27ms
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Sources: EU EUDAMED, US FDA
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FDA Adverse Event
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ELECTROSCOPE AEM CORD
FDA Adverse Event
Other
·ENCISION INC.·Product code GEI·August 9, 2000
LEEP SYSTEM 1000 ESU GEN
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code HGI·August 18, 2021
CUP: MPACT ACETABULAR SHELL 56 MULTI-HOLE
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·March 15, 2021
AMISTEM C FEMORAL STEMS
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·May 27, 2026
HEMASHIELD GOLD WOVEN D.V. AORTIC ARCH VASC.
FDA Adverse Event
Malfunction
·MAQUET CADIOVASCULAR, LLC·Product code DSY·March 8, 2013
COATED VICRYL PLUS (POLYGLACTIN 910) SUTURE
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code GAM·February 3, 2011
7700
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·February 20, 2008
88-000006 ROCKER W/COATED BLADE N/S
FDA Adverse Event
Malfunction
·DEROYAL·Product code GEI·December 8, 2000
RESTORE ULTRA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·October 28, 2014
CARPENTIER-MCCARTHY-ADAMS IMR ETLOGIX MITRAL ANNULOPLASTY RING
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code KRH·May 2, 2013
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·October 28, 2014
PRIMEADVANCED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·October 28, 2014
SINGLE USE BILIARY DRAINAGE STENT V
FDA Adverse Event
Injury
·AOMORI OLYMPUS CO., LTD.·Product code FGE·October 4, 2024
EVIS LUCERA DUODENOVIDEOSCOPE
FDA Adverse Event
Injury
·AIZU OLYMPUS CO., LTD.·Product code FDT·October 4, 2024
PRIMEADVANCED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·January 15, 2015
PRIMEADVANCED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·January 15, 2015
PRIMEADVANCED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·January 15, 2015
ADVANTAV12,COVERED STENTSYS, 6X59X120
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code NIO·January 12, 2026
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code MHY·June 28, 2018