340 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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COVERLOC VOLAR PLATE SHEATH, RADIAL, RIGHT
FDA Adverse Event
Malfunction
·DVO·Product code HRS·July 15, 2008
OPTICATH CVO CATHETER EXPANDED KIT
FDA Adverse Event
Malfunction
·ICU MEDICAL,INC.·Product code FPA·March 27, 2014
DW ARTHROSCOPY FLUID MANAGEMENT DEV
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HRX·October 15, 2025
ONE PIECE MAIN PUMP&PATIENT EXT TBG
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HRX·October 28, 2025
EVO MEDICAL'S AEROMAX 3002 NEBULIZER
FDA Adverse Event
Malfunction
·EVO MEDICAL SOLUTIONS·Product code CAF·December 1, 2008
EVO MEDICAL'S AEROMAX 3002 NEBULIZER
FDA Adverse Event
Malfunction
·EVO MEDICAL SOLUTIONS·Product code CAF·March 3, 2008
RAIN DROP NEAR VISION INLAY
FDA Adverse Event
Malfunction
·RVO 2.0, INC·Product code LQE·December 19, 2019
UNIVERSAL GLENOID CORRECTION REAMER
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 30, 2024
FLIPCUTTER II, SHORT 9.5MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HWE·May 20, 2024
SHAVER HP, APSII, HAND CONTROL
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HWE·May 7, 2024
ARTHREX ANGEL BMC KIT
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code ORG·June 12, 2024
BASEPLATE IMPACTOR, ASSEMBLY
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·January 24, 2022
BIO-COMP, SWIVELOCK C, FT, 4.75X19.1MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MAI·September 24, 2025
ACL TIGHTROPE WITH FIBERTAG
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HTY·December 29, 2023
Ø7X 20MM BC IF SCRW, VENTED
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MAI·December 31, 2024
T25 HEXALOBE, ISO, CANN.
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·July 3, 2023
SUTURE ANCHOR, BIO-CORKSCREW FT
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MAI·September 1, 2023
ACL REPAIR TIGHTROPE, WITH INTERNALBRACE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MBI·April 15, 2024
FASTPASS SCORPION
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·November 29, 2023
DW ARTHROSCOPY FLUID MANAGEMENT DEV
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HRX·June 11, 2024