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DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System 2160016Recalls & reported problems

Medtronic Sofamor Danek, Inc. · PLATE 2160016 ALIF PLATE 16MM · Class 2 · Implant

All models of DIVERGENCE-L Anterior/Oblique Lumbar Fusion System (14)

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 00643169502451), received between Nov 16, 2017 and Nov 16, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Migration or Expulsion of Device” (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

  • Migration or Expulsion of Device1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionNov 16, 2017Migration or Expulsion of Device; Migration or Expulsion of Device

    IT WAS REPORTED THAT POST-OP, PLATE MIGRATED ANTERIORLY. NO FUTURE SURGERY WAS PLANNED. NO PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THE EVENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7037754 ↗

Other Intervertebral fusion device with bone graft, lumbar devices

All Intervertebral fusion device with bone graft, lumbar devices →

Sources and updates

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