Intera Oncology Inc.

7 devices · 323 adverse event reports · 1 devices named in recalls

Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.

• INTERA AP-03000H

  Pump, Infusion, Implanted, Programmable
  2 recalls274 reports
• INTERA AP-07014US

  Non-Coring (Huber) Needle
  37 reports
• INTERA IP-37957

  Pump, Infusion, Implanted, Programmable
  3 reports
• INTERA AP-07004

  Non-Coring (Huber) Needle
  3 reports
• INTERA AP-07004

  Pump, Infusion, Implanted, Programmable
  3 reports
• INTERA AP-04013-5

  Non-Coring (Huber) Needle
  2 reports
• INTERA AP-04009

  Non-Coring (Huber) Needle
  1 report