13 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CAPSTONE® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·July 16, 2013
CAPSTONE® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK PUERTO RICO OPERATIONS·Product code MAX·November 18, 2013
CAPSTONE SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·October 26, 2018
CAPSTONE VERTEBRAL BODY SPACER
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code MQP·October 1, 2009
CAPSTONE VERTEBRAL BODY SPACER
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC INC.·Product code MAX·June 18, 2009
CAPSTONE SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·July 31, 2017
ACCU-CHEK ® MULTICLIX
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·March 5, 2013
SPRINT FIDELIS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code KRG·August 8, 2014
CORNERSTONE-SR CAGE SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code ODP·March 21, 2025
CORNERSTONE-SR CAGE SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code ODP·March 21, 2025
CAPSTONE® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code MAX·November 19, 2025
CAPSTONE® SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code MAX·July 21, 2023