8 results
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29ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
K012364
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JDI·February 3, 2015
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·February 12, 2025
CADD MEDICATION CASSETTE RESERVOIR
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC·Product code FPA·November 7, 2024
CADD EXTENSION SET
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC·Product code FPA·November 7, 2024
COAGUCHEK ® XS SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GJS·March 20, 2013
ACCU-CHEK ® INFORM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·March 9, 2011
APSII FOOTSWITCH, STANDARD
FDA Adverse Event
Other
·ARTHREX, INC.·Product code HWE·March 11, 2008
CADD-SOLIS VIP AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC·Product code FRN·November 7, 2024