Device, Neurovascular Embolization
FDA product code HCG · Class 2 · 1,223 devices · 11,944 reports · 37 deaths reported · 336 devices named in recalls
- Smart Coil 400SMTHXSFT1H02Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION58 reports
- POD RBYPODJ30Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION58 reports
- CEREPAK HELIFORM XHE120208Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall7 reports
- POD RBYPODJ45Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION57 reports
- Smart Coil 400SMTXSFT0410Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION56 reports
- CEREPAK FREEFORM XCR120515Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall5 reports
- CEREPAK FREEFORM XCR120406Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall4 reports
- CEREPAK FREEFORM XCR120408Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall4 reports
- CEREPAK FREEFORM XCR123505Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall4 reports
- CEREPAK FREEFORM XCR123509Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall4 reports
- CEREPAK UNIFORM FCX100730Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall4 reports
- Optima Coil System OPTI0152CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall3 reports
- Optima Coil System OPTI0306CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall3 reports
- Optima Coil System OPTI0408CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall3 reports
- Optima Coil System OPTI2065COM18Balt USA LLC · Device, Neurovascular Embolization1 recall3 reports
- CEREPAK FREEFORM MCR091525Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall3 reports
- CEREPAK FREEFORM SCR120721Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall3 reports
- CEREPAK FREEFORM XCR120202Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall3 reports
- CEREPAK FREEFORM XCR120510Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall3 reports
- CEREPAK FREEFORM XCR122505Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall3 reports
- HydroCoil Helical 140205HES-VMicrovention, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- Smart Coil 400SMTXSFT0206Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION52 reports
- LP Coil System RBYLP0105Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION52 reports
- Optima Coil System OPTI0204CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall2 reports
- Optima Coil System OPTI0254CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall2 reports
- Optima Coil System OPTI0308CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall2 reports
- Optima Coil System OPTI0408CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall2 reports
- Optima Coil System OPTI0620CST10Balt USA LLC · Device, Neurovascular Embolization1 recall2 reports
- Optima Coil System OPTI0254CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall2 reports
- Optima Coil System OPTI0620CST10Balt USA LLC · Device, Neurovascular Embolization1 recall2 reports
- CEREPAK FREEFORM SCR120410Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK FREEFORM SCR120620Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK HELIFORM SHD180312Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK FREEFORM XCR122535Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 death2 reports
- CEREPAK HELIFORM XHE120206Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK UNIFORM FCX100412Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK UNIFORM FCX100626Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK UNIFORM FCX100713Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK UNIFORM FCX181846Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- Penumbra Coil 400 4002C1040Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION52 reports
- Smart Coil 400SMTSFT0515Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION51 reports
- Optima Coil System OPTI0101CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0202CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0208CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0253CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0306CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0356CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0508CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0407CSF10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0413CSF10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0517CSF10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0620CSF10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI1027CST10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI2265COM18Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0102HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0620HST10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0204CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0253CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0517CST10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0816CST10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0827CST10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0930CST10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0620COM18Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI1240COM18Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI1860COM18Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI2265COM18Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0154HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0306HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0508HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0510HSS10Balt USA LLC · Device, Neurovascular Embolization1 recall1 report
- Optima Coil System OPTI0615HST10Balt USA LLC · Device, Neurovascular Embolization1 recall1 death1 report
- GALAXY G3 GLY120515Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION51 reports
- GALAXY G3 GLX120306Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION51 reports
- CEREPAK UNIFORM FCX182050Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM MCR092555Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM MCR093040Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM SCR120306Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM SCR120412Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM SCR120510Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM SCR120610Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM SCR120715Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK HELIFORM SHD180520Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM XCR120620Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM XCR122525Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK UNIFORM FCX181447Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK UNIFORM FCX180510Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM MCR092020Cerenovus, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- RUBY Coil RBY4C0415-APenumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION51 reports
- Optima Coil System OPTI0156BLKBalt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0258BLKBalt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- MicroPlex Helical Soft 100404HC-S-VMicrovention, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- Smart Coil 400SMTHXSFT0306Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION50 reports
- POD RBYPOD4-APenumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION50 reports
- Optima Coil System OPTI0103CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0104CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0152CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0153CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0154CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0203CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports
- Optima Coil System OPTI0304CSS10Balt USA LLC · Device, Neurovascular Embolization1 recall0 reports