7,347 results
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31ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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CADD-LEGACY PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FRN·July 23, 2018
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·March 10, 2023
GZ-130PA
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code DRT·June 12, 2023
EXCITEOSA
FDA Adverse Event
Malfunction
·SIGNIFIER MEDICAL TECHNOLOGIES LTD·Product code QNO·June 3, 2021
EXCITEOSA
FDA Adverse Event
Malfunction
·SIGNIFIER MEDICAL TECHNOLOGIES LTD·Product code QNO·June 28, 2021
EXCITEOSA
FDA Adverse Event
Malfunction
·UNKNOWN·Product code QNO·June 28, 2023
SIGNIFIER MEDICAL EXCITE OSA
FDA Adverse Event
Malfunction
·SIGNIFIER MEDICAL TECHNOLOGIES LIMITED·Product code QNO·March 11, 2022
PIPELINE VANTAGE WITH SHIELD TECHNOLOGY
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·May 6, 2024
ON-Q PAIN RELIEF SYSTEM WITH SELECT-A-FLOW, 400 ML, 2-14 ML/HR
FDA Adverse Event
Malfunction
·AVANOS MEDICAL INC.·Product code MEB·March 18, 2025
PUMP MMT-1780KPK 670G PATHWAY BLACK MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·August 6, 2021
PUMP MMT-1780KPK 670G PATHWAY BLACK MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 26, 2023
EVEREST BICOAG
FDA Adverse Event
Malfunction
·GYRUS ACMI·Product code GEI·April 18, 2017
PUMP MMT-1780KPK 670G PATHWAY BLACK MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 30, 2023
OPTIMA COIL SYSTEM
FDA Adverse Event
Malfunction
·BALT USA·Product code HCG·August 26, 2020
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 15, 2011
INO VENT
FDA Adverse Event
Malfunction
·INO THERAPEUTICS·Product code MRN·November 22, 2004
INO VENT
FDA Adverse Event
Malfunction
·INO THERAPEUTICS·Product code MRN·December 7, 2004
INO THERAPEUTICS
FDA Adverse Event
Malfunction
·INO THERAPEUTICS·Product code CBK·May 7, 2001
INO THERAPEUTICS
FDA Adverse Event
Malfunction
·INO THERAPEUTICS·Product code CBK·May 7, 2001
INO THERAPEUTICS
FDA Adverse Event
Malfunction
·INO THERAPEUTICS·Product code MRN·May 7, 2001