10 results
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31ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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TRYTON SIDE BRANCH STENT
FDA Adverse Event
Malfunction
·POSEIDON MEDICAL, INC.·Product code MAF·July 26, 2020
TRYTON SIDE BRANCH STENT
FDA Adverse Event
Malfunction
·TRYTON MEDICAL, INC.·Product code MAF·July 26, 2020
TRYTON SIDE BRANCH STENT
FDA Adverse Event
Injury
·POSEIDON MEDICAL, INC.·Product code MAF·April 9, 2020
TRYTON SIDE BRANCH STENT
FDA Adverse Event
Death
·TRYTON MEDICAL, INC.·Product code MAF·February 5, 2020
C2500MS & M2500-39 LALAPM
FDA Adverse Event
Injury
·STRYKER MEDICAL-KALAMAZOO·Product code IOQ·March 14, 2013
LIFEVEST WCD 3000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·November 14, 2008
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 15, 2011
4MM 30° C-MOUNT STYLE A ARTHROSCOPE
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY-SAN JOSE·Product code HRX·July 26, 2013
WISE CRT SYSTEM
FDA Adverse Event
Injury
·EBR SYSTEMS, INC·Product code SEG·September 5, 2025
BAROSTIM NEO2
FDA Adverse Event
Malfunction
·CVRX, INC·Product code DSR·July 9, 2024