10 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
16 X 100 MM X 8.5 ML BD VACUTAINER® SST II PLUS PLASTIC SERUM TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 29, 2017
BD VACUTAINER® SST II PLUS PLASTIC SERUM TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 3, 2017
16 X 100 MM X 8.5 ML BD VACUTAINER® SST II PLUS PLASTIC SERUM TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 27, 2017
BD VACUTAINER® SST II PLUS PLASTIC SERUM TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 27, 2017
MEGA NEEDLE DRIVER INSTRUMENT
FDA Adverse Event
Injury
·INTUITIVE SURGICAL,INC.·Product code NAY·March 19, 2013
ACCU-CHEK FLEXLINK PLUS INFUSION SET
FDA Adverse Event
Injury
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·March 4, 2011
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 10, 2008
REAMER SHAFT, AO FITTING BIXCUT Ø8,0X448 MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·October 23, 2017
REAMER SHAFT, AO FITTING BIXCUT Ø8,0X448 MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·October 23, 2017
REAMER SHAFT, AO FITTING BIXCUT Ø8,0X448 MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·October 23, 2017