7 results
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24ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 23, 2016
M.U.S.T. MIDLINE CORTICAL (MC) SCREW SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·July 11, 2025
MYSPINE
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code PQC·September 27, 2024
LIFEVEST WCD 3000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·October 20, 2008
PEDICLE SCREW MUST MC SCREW Ø6X45
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·December 21, 2022
RIGIDFIX FEM2.7MM B/T/B XPIN
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·May 3, 2021
RIGIDFIX FEM2.7MM B/T/B XPIN
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·January 25, 2019