Skip to content

ALEUTIAN® Interbody Systems 702-90178Recalls & reported problems

VB Spine LLC · Lordotic Trial, Size 28x36x17 mm, 15° · Class 2

All models of ALEUTIAN Interbody Systems (37)

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 10888857128002), received between Feb 3, 2022 and Feb 3, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical Jam” (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

  • Mechanical Jam1

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.

  • MalfunctionFeb 3, 2022Mechanical Jam; Mechanical Jam

    IT WAS REPORTED THAT AN ANTERIOR LUMBAR DISC PREP LORDOTIC TRIAL BECAME STUCK ON AND INSERTER AND INNER SHAFT DURING INTRA-OPERATIVE TRIALING. 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 13446893 ↗

Other Intervertebral fusion device with bone graft, cervical devices

All Intervertebral fusion device with bone graft, cervical devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page