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

• MicroNester G52738

  Cook Incorporated · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• MicroNester G52739

  Cook Incorporated · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• MicroNester G52741

  Cook Incorporated · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• Prestige Coil System PRES0827COM18

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall0 reports
• Prestige Coil System PRES1034COM18

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall0 reports
• Prestige Coil System PRES1240COM18

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall0 reports
• Prestige Coil System PRES1447COM18

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall0 reports
• Prestige Coil System PRES1860COM18

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall0 reports
• Prestige Coil System PRES2065COM18

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall0 reports
• Prestige Coil System PRES2465COM18

  Balt USA LLC · Device, Vascular, For Promoting Embolization
  1 recall0 reports
• CEREPAK FREEFORM SCR122505

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK FREEFORM SCR123575

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM SHD100208

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM SHD100408

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM SHD100510

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM SHD100515

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM SHD100612

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM SHD100616

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM SHD100716

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM SHD100820

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM SHD180835

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM SHD180935

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM SHD181650

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM SHD181855

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM SHD182260

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK FREEFORM XCR120201

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM XHD100151

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM XHD100201

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM XHD100202

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM XHD100204

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM XHD100256

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM XHD100304

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK HELIFORM XHD100306

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX100305

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX100253

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX100611

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX100829

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK Uniform FCX141127

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK Uniform FCX141230

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX140306

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX140408

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX140507

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX140717

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX140812

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX140914

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX181034

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX181240

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX181550

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX181647

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX181750

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX180612

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• CEREPAK UNIFORM FCX180830

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 recall0 reports
• RUBY Coil RBY4C0315-B

  Penumbra, Inc. · Device, Vascular, For Promoting Embolization
  49 reports
• Concerto Detachable Coil System NV-2-4-HELIX

  Micro Therapeutics, Inc. · Device, Vascular, for Promoting Embolization
  2 deaths46 reports
• Interlock™ M001361570

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  46 reports
• Azur CX Detachable 45-751019

  Microvention, Inc. · Device, Vascular, for Promoting Embolization
  44 reports
• Interlock™ M001361960

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  44 reports
• RUBY Coil RBY2C1260-B

  Penumbra, Inc. · Device, Vascular, For Promoting Embolization
  42 reports
• RUBY Coil RBY4C0415-B

  Penumbra, Inc. · Device, Vascular, For Promoting Embolization
  41 reports
• ORBIT GALAXY XTRASOFT 640CX0306

  Medos International Sàrl · Device, Vascular, for Promoting Embolization
  41 reports
• DELTAXSFT DLX100206

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  39 reports
• AxiumTM APB-3-6-3D-ES

  Micro Therapeutics, Inc. · Device, Vascular, for Promoting Embolization
  36 reports
• POD RBYPOD5-A

  Penumbra, Inc. · Device, Vascular, For Promoting Embolization
  35 reports
• Concerto Detachable Coil System NV-6-20-HELIX

  Micro Therapeutics, Inc. · Device, Vascular, for Promoting Embolization
  35 reports
• TARGET M0035421540

  Stryker Corporation · Device, Vascular, for Promoting Embolization
  35 reports
• Interlock™ M001361580

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  35 reports
• ORBIT GALAXY XTRASOFT 640CX2505

  Medos International Sàrl · Device, Vascular, for Promoting Embolization
  35 reports
• POD RBYPODJ5-A

  Penumbra, Inc. · Device, Vascular, For Promoting Embolization
  34 reports
• RUBY Coil RBY4C0204-B

  Penumbra, Inc. · Device, Vascular, For Promoting Embolization
  34 reports
• Interlock™ M001361530

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  34 reports
• Interlock™-35 M001363650

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  34 reports
• Concerto Detachable Coil System NV-3-4-HELIX

  Micro Therapeutics, Inc. · Device, Vascular, for Promoting Embolization
  1 death33 reports
• TARGET M0035421020

  Stryker Corporation · Device, Vascular, for Promoting Embolization
  33 reports
• TARGET XL M0036128300

  Stryker Corporation · Device, Vascular, for Promoting Embolization
  1 death33 reports
• Interlock™-35 M001363670

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  33 reports
• GALAXY G3 GLY120308

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  33 reports
• IMPEDE-FX Embolization Plug IMP-FX-12

  Shape Memory Medical Inc. · Device, Vascular, For Promoting Embolization
  5 deaths32 reports
• ConcertoTM NV-2-8-HELIX

  Micro Therapeutics, Inc. · Device, Vascular, for Promoting Embolization
  32 reports
• Embosphere® 00884450402948

  Biosphere Medical · Device, Vascular, for Promoting Embolization
  1 death32 reports
• TARGET XL M0036121040

  Stryker Corporation · Device, Vascular, for Promoting Embolization
  32 reports
• Interlock™-35 M001363550

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  32 reports
• DELTAFILL DLF180415

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  32 reports
• GALAXY G3 GLX120202

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  3 deaths32 reports
• GALAXY G3 GLX120410

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  32 reports
• GALAXY G3 GLX120408

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  32 reports
• GALAXY G3 GLM930060

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  1 death32 reports
• AMPLATZER™ 9-AVP2-008

  Aga Medical Corporation · Device, Vascular, for Promoting Embolization
  31 reports
• RUBY Coil RBY4C0835-B

  Penumbra, Inc. · Device, Vascular, For Promoting Embolization
  31 reports
• AxiumTM APB-2-4-3D-ES

  Micro Therapeutics, Inc. · Device, Vascular, for Promoting Embolization
  31 reports
• Concerto Detachable Coil System NV-5-20-HELIX

  Micro Therapeutics, Inc. · Device, Vascular, for Promoting Embolization
  1 death31 reports
• TARGET XL M0036126200

  Stryker Corporation · Device, Vascular, for Promoting Embolization
  31 reports
• Interlock™ M001361920

  Boston Scientific Corporation · Device, Vascular, for Promoting Embolization
  31 reports
• DELTAFILL DLF180625

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  30 reports
• RUBY Coil RBY4C0630-B

  Penumbra, Inc. · Device, Vascular, For Promoting Embolization
  29 reports
• Concerto Detachable Coil System NV-8-30-HELIX

  Micro Therapeutics, Inc. · Device, Vascular, for Promoting Embolization
  2 deaths29 reports
• DELTAFILL DLF180312

  Cerenovus, Inc. · Device, Vascular, for Promoting Embolization
  29 reports
• Azur CX Detachable 45-780413

  Microvention, Inc. · Device, Vascular, for Promoting Embolization
  28 reports
• AMPLATZER™ 9-AVP2-010

  Aga Medical Corporation · Device, Vascular, for Promoting Embolization
  1 death28 reports
• AMPLATZER™ 9-AVP2-012

  Aga Medical Corporation · Device, Vascular, for Promoting Embolization
  28 reports
• Azur CX Detachable 45-751632

  Microvention, Inc. · Device, Vascular, for Promoting Embolization
  28 reports