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Avenue L IR90021RRecalls & reported problems

LDR Spine Usa, Inc. · AVENUE-L ANCH PLATE IMPACTOR · Class 2

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 03662663039642), received between Nov 15, 2021 and Nov 15, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Physical Resistance/Sticking” (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

  • Physical Resistance/Sticking1

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.

  • MalfunctionNov 15, 2021Physical Resistance/Sticking; Physical Resistance/Sticking

    IT WAS REPORTED THAT A CAGE HOLDER, IMPACTOR, AND PLATE ALL BECAME JAMMED TOGETHER DURING SURGERY AND COULD NOT BE DISASSEMBLED. THERE WAS A DELAY ASSOCIATED WITH TRYING TO GET THE HOLDER AND IMPACTOR UNSTUCK FROM THE PLATE, BUT THERE WERE NO IMPACTS TO THE PATIENT. THIS IS REPORT THREE OF THREE FOR THIS EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12817160 ↗

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Sources and updates

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