8 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OT VERIO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 2, 2011
FLO-GARD 6201 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE (SG)·Product code FRN·November 18, 2008
HAKIM VENTRICULAR & PERIOTNEAL CATHETERS WITH BACTISEAL
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code JXG·July 18, 2013
IMMULITE 2000 ESTRADIOL
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code CHP·December 6, 2024
OT SELECT MINI METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·September 18, 2012
PROTEGE EVERFLEX SELF-EXPANDING STENT SYSTEM LONG
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FGE·March 13, 2019
IMMULITE 2000 ESTRADIOL
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code CHP·December 6, 2024
IMMULITE 2000 ESTRADIOL
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code CHP·December 6, 2024