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CASCADIA™ Interbody System 6101-2852808NL12-G2Recalls & reported problems

VB Spine LLC · 6101-2852808NL12-G2 · Class 2 · Implant

All models of CASCADIA Interbody System (28)

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

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888857316355), received between Dec 15, 2021 and Dec 15, 2021 — 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

Device problems

  • Fracture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionDec 15, 2021Fracture; Fracture

    IT WAS REPORTED THAT DURING ROTATION OF A CASCADIA AN INTERBODY IN L5, THE IMPLANT "BROKE IN HALF". HALF OF THE IMPLANT WAS LEFT IN THE PATIENT AND THE OTHER HALF WAS RETAINED BY THE HOSPITAL. SURGERY WAS SUCCESSFULLY COMPLETED WITH A 10 MINUTE DELAY. NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13011917 ↗

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Sources and updates

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