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CASCADIA™ Interbody System 7908-42F223Recalls & reported problems

VB Spine LLC · Cayman United 2 Hole Plate, Size 22 · Class 2 · Implant

All models of CASCADIA Interbody System (28)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888857369153), received between Sep 30, 2021 and Dec 6, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (2 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 18, 2026.

Most reported problems

Device problems

  • Insufficient Device Problem Information2
  • Adverse Event Without Identified Device or Use Problem1
  • Device Dislodged or Dislocated1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionDec 6, 2022Device Dislodged or Dislocated; Insufficient Device Problem Information; Device Dislodged or Dislocated; Insufficient Device Problem Information

    IT WAS REPORTED THAT A CAYMAN UNITED SCREW "WENT THROUGH" A CASCADIA CAYMAN UNITED TWO-HOLE PLATE INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A TEN-MINUTE SURGICAL DELAY WITH NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT CAPTURES THE CAYMAN UNITED TWO-HOLE PLATE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15924295 ↗
  • MalfunctionSep 30, 2021Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

    IT WAS REPORTED THAT THE TIP OF THE CAYMAN MI SPRING LOADED AWL BENT INTRA-OPERATIVELY. THE AWL IS USED TO PREPARE THE BONE FOR PLACEMENT OF SCREWS. THE SURGEON DID NOT ELECT TO USE OR DID NOT HAVE ON HAND A BACK-UP INSTRUMENT TO PREPARE THE SECOND SCREW HOLE. THE CAYMAN UNITED TWO-HOLE PLATE AND CASCADIA INTERBODY WERE IMPLANTED BUT ONLY ONE OF TWO SECURING SCREWS WAS PLACED. NO ADVERSE CONSEQUENCES TO THE PATIENT HAVE BEEN REPORTED AND THE SURGEON DOES NOT PLAN TO RE-OPERATE AT THIS TIME. THIS RECORD CAPTURES THE CAYMAN UNITED TWO-HOLE PLATE IMPLANTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12558228 ↗

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Sources and updates

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