CASCADIA™ Interbody System 7902-90033Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10888857383708), received between Sep 13, 2021 and Apr 17, 2025 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (4 reports).

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 16, 2026.

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 17, 2025Difficult to Insert; Mechanical Problem; Difficult to Insert; Mechanical Problem

  NO NEW INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21862606 ↗
• MalfunctionJul 11, 2022Mechanical Problem; Mechanical Problem

  A COMPANY REPRESENTATIVE REPORTED THAT OUTSIDE THE OPERATING ROOM A CASCADIA LATERAL PLATE INSERTER WOULD NOT PROPERLY HOLD THE PLATE. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT. SURGERY WAS COMPLETELY SUCCESSFULLY WITHOUT SURGICAL DELAY BY USING AN ALTERNATIVELY AVAILABLE DEVICE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14977960 ↗
• MalfunctionMay 23, 2022Fracture; Material Deformation; Fracture; Material Deformation

  IT WAS REPORTED THAT A CASCADIA LATERAL INSERTER BROKE AT THE TIP OUTSIDE THE OR. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14470786 ↗
• MalfunctionMar 2, 2022Mechanical Jam; Failure to Eject; Mechanical Jam; Failure to Eject

  A COMPANY REPRESENTATIVE REPORTED THAT A CAYMAN UNITED INSERTER WOULD NOT RELEASE FROM THE IMPLANT DURING SURGERY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13654428 ↗
• MalfunctionNov 22, 2021Difficult or Delayed Positioning; Mechanical Problem; Difficult or Delayed Positioning; Mechanical Problem

  IT WAS REPORTED THAT OUTSIDE THE OR A CAYMAN UNITED PLATE INSERTER WILL NO LONGER SECURELY HOLD PLATES. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12857737 ↗
• MalfunctionSep 30, 2021Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT OUTSIDE THE OR, THE CAYMAN UNITED PLATE INSERTER WON'T RELEASE FROM PLATE WHEN LOOSENED. THERE IS NO PROCEDURE ASSOCIATED WITH THIS REPORTED EVENT, NO PATIENT INVOLVEMENT, AND NO ADVERSE CONSEQUENCE HAS BEEN REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12558384 ↗
• MalfunctionSep 13, 2021Mechanical Problem; Mechanical Problem

  IT WAS REPORTED THAT THE CAYMAN UNITED PLATE INSERTER DID NOT HOLD FIRMLY TO THE CAGE, MAKING IT DIFFICULT TO INSERT. NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED.  THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 60 MINUTE SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12460493 ↗