Device, Vascular, for Promoting Embolization

FDA product code KRD · Class 2 · 1,534 devices · 9,607 reports · 87 deaths reported · 332 devices named in recalls

• POD RBYPOD8-A

  Penumbra, Inc. · Device, Vascular, For Promoting Embolization
  195 reports
• CEREPAKTM MDH1

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall72 reports
• Azur CX Detachable 45-750824

  Microvention, Inc. · Device, Vascular, for Promoting Embolization
  115 reports
• Tornado G08261

  Cook Incorporated · Device, Vascular, for Promoting Embolization
  2 recalls7 reports
• Optima Coil System OPTI0720CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls4 reports
• Optima Coil System OPTI0930CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls4 reports
• Optima Coil System OPTI0413CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls3 reports
• Prestige Coil System PRES0520HPKPL

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls3 reports
• Optima Coil System OPTI0407CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls2 reports
• Optima Coil System OPTI4510CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls2 reports
• Optima Coil System OPTI0202CSSMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls1 report
• Optima Coil System OPTI0307CSSMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls1 report
• Optima Coil System OPTI0310CSSMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls1 report
• Optima Coil System OPTI0510CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls1 report
• Optima Coil System OPTI1040CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls1 report
• Optima Coil System OPTI1650CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls1 report
• Optima Coil System OPTI0520CSF10

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls1 report
• Tornado G08357

  Cook Incorporated · Device, Vascular, for Promoting Embolization
  2 recalls1 report
• Optima Coil System OPTI0255CSSMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Optima Coil System OPTI3535CSSMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Optima Coil System OPTI0404CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Optima Coil System OPTI4545CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Optima Coil System OPTI0507CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Optima Coil System OPTI0715CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Optima Coil System OPTI1245CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Optima Coil System OPTI1445CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Optima Coil System OPTI0153HSSMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Prestige Coil System PRES0153HXPPL

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Prestige Coil System PRES0315HXPPL

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Prestige Coil System PRES0420HPKPL

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Prestige Coil System PRES0720HPKPL

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Prestige Coil System PRES0830HPKPL

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Prestige Coil System PRES0204CXPPL

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Prestige Coil System PRES0307CXPPL

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  2 recalls0 reports
• Interlock™-35 M001363830

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  98 reports
• Azur CX Detachable 45-751324

  Microvention, Inc. · Device, Vascular, for Promoting Embolization
  1 recall42 reports
• Interlock™-35 M001363590

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  92 reports
• GALAXY G3 GLM920060

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  89 reports
• Interlock™-35 M001363800

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  86 reports
• Concerto Detachable Coil System NV-3-8-HELIX

  Micro Therapeutics, Inc. · Device, Vascular, for Promoting Embolization
  81 reports
• Concerto Detachable Coil System NV-2-8-HELIX

  Micro Therapeutics, Inc. · Device, Vascular, for Promoting Embolization
  79 reports
• GALAXY G3 GLM910030

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  79 reports
• GALAXY G3 GLM910040

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  77 reports
• OBSIDIO™ M0013972101010

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  1 recall26 reports
• Azur CX Detachable 45-750617

  Microvention, Inc. · Device, Vascular, for Promoting Embolization
  76 reports
• Interlock™-35 M001363630

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  72 reports
• POD RBYPOD10-A

  Penumbra, Inc. · Device, Vascular, For Promoting Embolization
  71 reports
• Concerto Detachable Coil System NV-2-6-HELIX

  Micro Therapeutics, Inc. · Device, Vascular, for Promoting Embolization
  4 deaths71 reports
• Interlock™-35 M001363820

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  1 death65 reports
• CEREPAK FREEFORM MCR091020

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall12 reports
• CEREPAK FREEFORM MCR092060

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall12 reports
• Interlock™-35 M001363610

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  60 reports
• CEREPAK FREEFORM MCR091040

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall10 reports
• CEREPAK FREEFORM MCR092030

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall8 reports
• CEREPAK FREEFORM XCR120304

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall7 reports
• CEREPAK FREEFORM XCR120308

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall7 reports
• CEREPAK FREEFORM XCR120410

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall7 reports
• RUBY Coil RBY4C0860-B

  Penumbra, Inc. · Device, Vascular, For Promoting Embolization
  56 reports
• Optima Coil System OPTI0620CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall6 reports
• CEREPAK FREEFORM MCR091030

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall6 reports
• CEREPAK FREEFORM MCR091530

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall6 reports
• CEREPAK FREEFORM MCR092040

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall6 reports
• CEREPAK FREEFORM XCR120306

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall6 reports
• OBSIDIO™ M0013972001010

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  1 recall2 deaths5 reports
• Azur CX Detachable 45-752039

  Microvention, Inc. · Device, Vascular, for Promoting Embolization
  55 reports
• TARGET M0035421030

  Stryker Corporation · Device, Vascular, for Promoting Embolization
  55 reports
• CEREPAK FREEFORM MCR091540

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall5 reports
• CEREPAK FREEFORM MCR093060

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall5 reports
• CEREPAK UNIFORM FCX100356

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall5 reports
• Optima Coil System OPTI0152CSSMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall4 reports
• Optima Coil System OPTI0517CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall4 reports
• Optima Coil System OPTI0615CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall4 reports
• CEREPAK FREEFORM SCR120407

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall4 reports
• CEREPAK UNIFORM FCX100407

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall4 reports
• Prestige Coil System PRES0320CXPPLT

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall3 reports
• Optima Coil System OPTI0830CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall3 reports
• Tornado G08259

  Cook Incorporated · Device, Vascular, for Promoting Embolization
  1 recall3 reports
• CEREPAK FREEFORM SCR120615

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall3 reports
• CEREPAK UNIFORM FCX100517

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall3 reports
• Prestige Coil System PRES0204CXPPLT

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall2 reports
• Prestige Coil System PRES3530CXPPLT

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall2 reports
• Prestige Coil System PRES0635CPKPLT

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall2 reports
• Optima Coil System OPTI2525CSSMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall1 death2 reports
• Optima Coil System OPTI0611CSFMX

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall2 reports
• Optima Coil System OPTI0615CSF10

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall2 reports
• Prestige Coil System PRES0103CXPPL

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall2 reports
• Tornado G08356

  Cook Incorporated · Device, Vascular, for Promoting Embolization
  1 recall2 reports
• MicroNester G52731

  Cook Incorporated · Device, Vascular, for Promoting Embolization
  1 recall2 reports
• MicroNester G52732

  Cook Incorporated · Device, Vascular, for Promoting Embolization
  1 recall2 reports
• AxiumTM QC-4-12-HELIX

  Micro Therapeutics, Inc. · Device, Vascular, for Promoting Embolization
  1 recall2 reports
• AxiumTM QC-10-30-3D

  Micro Therapeutics, Inc. · Device, Vascular, for Promoting Embolization
  1 recall2 reports
• INZONE M00345100950

  Stryker Corporation · Device, Vascular, for Promoting Embolization
  1 recall2 reports
• CEREPAK FREEFORM SCR121230

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall2 reports
• CEREPAK HELIFORM SHD180415

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall2 reports
• CEREPAK FREEFORM XCR123575

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall2 reports
• CEREPAK HELIFORM XHE120204

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall2 reports
• CEREPAK UNIFORM FCX100509

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall2 reports
• CEREPAK UNIFORM FCX180714

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall2 reports
• Prestige Coil System PRES0310CXPPLT

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall1 report
• Prestige Coil System PRES0420CPKPLT

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall1 report