10 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
DRIVER SHAFT, T10, NON-RETAINING
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·July 17, 2024
DRIVER SHAFT, T10, NON-RETAINING
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·August 8, 2023
DRIVER SHAFT, T10, NON-RETAINING
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·October 7, 2024
DRIVER SHAFT, T10, NON-RETAINING
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 13, 2026
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 17, 2019
GALAXY INTRAVASCULAR ULTRASOUND SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT (CE)·Product code IYO·December 19, 2012
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·October 13, 2010
HAND PIECE FOR BATTERY POWERED DRIVER
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HWE·October 21, 2025
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·July 26, 2018
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·February 27, 2025