14 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
ARTHREX INSERTION DEVICE FOR ARTHREX KNOTLESS FIBERTAK (2.6 FRENCH) SOFT ANCHOR
FDA Adverse Event
Malfunction
·ARTHREX INC.·Product code MBI·November 2, 2023
MEDLINE
FDA Adverse Event
Malfunction
·MEDLINE INDUSTRIES INC.·Product code ITJ·August 20, 2002
SUBLIME¿ RADIAL ACCESS 018 RX PTA DILATATION CATHETER
FDA Adverse Event
Malfunction
·CREAGH MEDICAL·Product code LIT·May 14, 2025
SUBLIME RADIAL ACCESS GUIDE SHEATH
FDA Adverse Event
Malfunction
·CREAGH MEDICAL·Product code DYB·April 1, 2022
UNK
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·January 10, 2024
SUBLIME¿ RADIAL ACCESS 018 RX PTA DILATATION CATHETER
FDA Adverse Event
Malfunction
·SURMODICS, INC.·Product code LIT·August 12, 2025
SUBLIME¿ RADIAL ACCESS 018 RX PTA DILATATION CATHETER
FDA Adverse Event
Malfunction
·CREAGH MEDICAL LTD.·Product code LIT·October 30, 2025
SUBLIME RADIAL ACCESS 018 RXPTA DILATATION CATHETER
FDA Adverse Event
Malfunction
·CREAGH MEDICAL·Product code LIT·April 1, 2022
SUBLIME¿ RADIAL ACCESS 018 RX PTA DILATATION CATHETER
FDA Adverse Event
Malfunction
·CREAGH MEDICAL·Product code LIT·February 16, 2023
SUBLIME¿ RADIAL ACCESS 018 RX PTA DILATATION CATHETER
FDA Adverse Event
Malfunction
·CREAGH MEDICAL·Product code LIT·March 15, 2023
SUBLIME¿ RADIAL ACCESS 018 RX PTA DILATATION CATHETER
FDA Adverse Event
Malfunction
·CREAGH MEDICAL·Product code LIT·September 25, 2023
SUBLIME¿ RADIAL ACCESS 018 RX PTA DILATATION CATHETER
FDA Adverse Event
Malfunction
·CREAGH MEDICAL·Product code LIT·May 20, 2025
UNSPECIFIED BD CPT BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JKA·September 14, 2022
ARTHREX ARTHROSCOPY PUMP TUBING
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HRX·July 1, 2019