Avenue L IR6002TRecalls & reported problems
LDR Spine Usa, Inc. · Avenue L Anchoring plate M · Class 2
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 03662663008327), received between Jun 2, 2021 and Jan 11, 2024 — classified as 2 malfunctions.
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.
Reports received per month
Most reported problems
Device problems
- Mechanical Jam1
- Mechanical Problem1
- Migration1
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.
MalfunctionJan 11, 2024Mechanical Problem; Migration; Mechanical Problem; Migration
IT WAS REPORTED THAT AN AVENUE L PLATE SEEMS TO HAVE BACKED OUT A LITTLE FROM THE CAGE POST-OPERATIVELY. THERE IS NO REVISION SURGERY PLANNED AS THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18499241 ↗MalfunctionJun 2, 2021Mechanical Jam; Mechanical Jam
IT WAS REPORTED THAT WHILE THE SURGEON WAS IMPACTING THE SECOND PLATE, IT DID NOT GO INTO THE CORRECT SLOT IN THE CAGE HOLDER; IT STARTED TO GO INTO THE FIRST PLATE'S SLOT AND BECAME JAMMED. THE PLATE COULD NOT BE REMOVED WHILE THE HOLDER WAS ATTACHED TO THE CAGE, SO THE CAGE AND FIRST PLATE WERE REMOVED WITH THE HOLDER. THE PLATE WAS THEN REMOVED FROM THE CAGE HOLDER AND A NEW CAGE AND PLATES WERE INSTALLED TO COMPLETE THE PROCEDURE. THERE WAS NO PATIENT IMPACT OR SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11924269 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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