CASCADIA™ Interbody System 6101-90170Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888857261129), received between Dec 18, 2023 and Dec 18, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 18, 2023Fracture; Fracture

  IT WAS REPORTED THAT DURING THE INSERTION OF A CASCADIA OBLIQUE INTERBODY AS THE SURGEON ATTEMPTED TO ROTATE THE CAGE, THE TIP OF A CASCADIA LORDOTIC - OBLIQUE INSERTER AND A THREAD FROM THE TIP OF AN ALEUTIAN INSERTER INNER SHAFT FRACTURED INTRA-OPERATIVELY. THE BROKEN PIECES WERE RETRIEVED AND X-RAYS CONFIRMED THAT THERE WERE NO ARTIFACTS LEFT IN PATIENT. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 15 MINUTE SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT IS FOR THE CASCADIA LORDOTIC - OBLIQUE INSERTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18352164 ↗