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Vu aPod™ - L 31-23-1245-12Recalls & reported problems

Seaspine Orthopedics Corporation · LATERAL IMPLANT, WIDE, LORDOTIC, 12mm X 23mm X 45mm X 12° · Class 2

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889981046699), received between Feb 26, 2018 and Feb 26, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Mechanical Problem” (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 Problem1
  • Migration or Expulsion of Device1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • InjuryFeb 26, 2018Mechanical Problem; Migration or Expulsion of Device; Mechanical Problem; Migration or Expulsion of Device

    PATIENT HAD PREVIOUS FUSION SURGERY FROM S1-L4 WITH POSTERIOR FIXATION; DATE UNKNOWN. ON (B)(6) 2018, PATIENT UNDERWENT LATERAL INTERBODY FUSION SURGERY ON L3-L4 WITH NO FIXATION AT L3-L4. ON (B)(6) 2018 IT WAS DISCOVERED THAT THE INTERBODY HAD MIGRATED LATERALLY OUTSIDE THE VERTEBRAL BODY AT L3-L4. REVISION SURGERY WAS PERFORMED TO REMOVE AND REPLACE THE DEVICE. POSTERIOR FIXATION WAS ADDED.

    Patient problems: Failure of Implant

    MAUDE report 7298106 ↗

Other Intervertebral fusion device with integrated fixation, lumbar devices

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Sources and updates

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