Implantable transprostatic tissue retractor system

FDA product code PEW · Class 2 · 15 devices · 284 reports · 11 deaths reported · 2 devices named in recalls

• UroLift UL400-4

  Neotract, Inc. · Implantable Transprostatic Tissue Retractor System
  1 recall9 deaths144 reports
• UroLift UL400-4

  Neotract, Inc. · Implantable Transprostatic Tissue Retractor System
  1 recall3 reports
• UROLIFT IPN924184

  Teleflex Incorporated · Implantable transprostatic tissue retractor system
  1 death32 reports
• UROLIFT IPN918876

  Teleflex Incorporated · Implantable transprostatic tissue retractor system
  18 reports
• UROLIFT IPN055826

  Teleflex Incorporated · Implantable transprostatic tissue retractor system
  15 reports
• UROLIFT IPN923352

  Teleflex Incorporated · Implantable transprostatic tissue retractor system
  15 reports
• UROLIFT IPN056134

  Teleflex Incorporated · Implantable transprostatic tissue retractor system
  1 death10 reports
• UROLIFT IPN056885

  Teleflex Incorporated · Implantable transprostatic tissue retractor system
  10 reports
• UROLIFT IPN919209

  Teleflex Incorporated · Implantable transprostatic tissue retractor system
  9 reports
• UROLIFT IPN056625

  Teleflex Incorporated · Implantable transprostatic tissue retractor system
  8 reports
• UROLIFT IPN924185

  Teleflex Incorporated · Implantable transprostatic tissue retractor system
  6 reports
• UROLIFT IPN923351

  Teleflex Incorporated · Implantable transprostatic tissue retractor system
  4 reports
• UROLIFT IPN929207

  Teleflex Incorporated · Implantable transprostatic tissue retractor system
  4 reports
• UROLIFT IPN056288

  Teleflex Incorporated · Implantable transprostatic tissue retractor system
  3 reports
• UROLIFT IPN929371

  Teleflex Incorporated · Implantable transprostatic tissue retractor system
  3 reports