9 results
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35ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
POINTED REDUCTION FORCEPS
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·February 7, 2022
DRIVER SHAFT, T6, NON-RETAINING, AO
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 17, 2024
SOLID SCREWDRIVER, T6 HEXALOBE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 17, 2024
DRIVER SHAFT, T6, SELF RETAINING, AO
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 17, 2024
DRIVER SHAFT, T6, NON-RETAINING, AO
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 17, 2024
DRIVER SHAFT, T6, SELF RETAINING, AO
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 17, 2024
POINTED REDUCTION FORCEPS
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 17, 2024
ILS 25MM CURVED
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 12, 2014
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·December 12, 2012