Device, Neurovascular Embolization
FDA product code HCG · Class 2 · 1,223 devices · 11,944 reports · 37 deaths reported · 336 devices named in recalls
- Optima Coil System OPTI0201HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0203HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0206HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0253HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0254HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0304HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0310HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0406HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0410HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0506HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0304HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0306HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0308HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0310HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0315HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0406HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0408HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0410HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0420HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0506HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0508HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0510HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0520HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0606HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0608HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0610HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0610HSF10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0620HST10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0720HST10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0730HST10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0820HST10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0830HST10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0930HST10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- CEREPAK FREEFORM MCR091010Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM MCR091025Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM MCR091520Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM MCR093080Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR120202Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR120515Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR120815Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR120824Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR120925Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR122535Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR123509Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100154Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100250Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100258Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100308Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100310Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100410Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100720Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100925Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD180625Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD180733Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD181040Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD181242Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD182060Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD182460Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM XHD100152Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM XHD100153Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM XHD100203Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM XHD100206Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM XHD100254Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM XHD100406Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM XHD100408Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX100202Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX100816Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX141016Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX141025Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX141118Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK Uniform FCX141219Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140225Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140303Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140304Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140445Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140406Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140512Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140615Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140609Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140711Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140820Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140922Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX181137Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX181220Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX181343Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX181950Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX180813Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX180915Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX180933Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- TARGET M0035442040Stryker Corporation · DEVICE, NEUROVASCULAR EMBOLIZATION49 reports
- RUBY Coil RBY4C0204-APenumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION49 reports
- RUBY Coil RBY4C1650-APenumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION49 reports
- GALAXY G3 GLM920030Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION48 reports
- RUBY Coil RBY2C0530-APenumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION48 reports
- Smart Coil 400SMTXSFT1H03Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION47 reports
- Smart Coil 400SMTXSFT0304Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION47 reports
- GALAXY G3 GLM920040Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION47 reports
- Penumbra Coil 400 4002C1660Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION47 reports
- RUBY Coil RBY2C1857-APenumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION47 reports
- Smart Coil 400SMTHXSFT0206Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION46 reports