10 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 6, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 6, 2024
HS III PROXIMAL SEAL SYSTEM 3.8MM
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code DXC·April 9, 2014
ZIMMER DERMATOME BLADE
FDA Adverse Event
Malfunction
·ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS·Product code GFD·October 1, 2010
TI MATRIX LOCKING CAP
FDA Adverse Event
Death
·SYNTHES BRANDYWINE·Product code NKB·December 20, 2012
ELEVATE¿ SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code MAX·May 20, 2024
ELEVATE¿ SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code MAX·January 30, 2025
ELEVATE¿ SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code MAX·July 31, 2023
ELEVATE SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code MAX·August 5, 2024
ELEVATE¿ SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code MAX·May 20, 2025