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X-MESH 188902028Recalls & reported problems

Medos International Sàrl · X-MESH EXPANDABLE CAGE SYSTEM EXPANDABLE VERTEBRAL BODY REPLACEMENT, LATERAL, LARGE 28 - 38mm, 0/0 DEGREES · Class 2 · Implant

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 10705034159928), received between Jan 2, 2018 and Jan 2, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Collapse” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Collapse1

Patient problems

  • Not Applicable1
  • Spinal Column Injury1

Recent adverse event reports

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

  • InjuryJan 2, 2018Collapse; Collapse

    CAGE COLLAPSED POST-OP WHEN WE LOOKED AT FILM NEXT DAY. PATIENT CONSEQUENCE? :YES. PATIENT CONSEQUENCE DESCRIPTION:LONGER ANESTHESIA, LONGER SURGERY. ACTION TAKEN FOR PROCEDURE:COMPRESSED POSTERIOR ELEMENTS AND RE-ALIGNED PATIENT CAGE. IS THE INFORMATION BEING SUBMITTED FOR THIS COMPLAINT ALL THE DETAILS THAT ARE KNOWN/AVAILABLE REGARDING THIS EVENT? : YES.

    Patient problems: Not Applicable; Spinal Column Injury

    MAUDE report 7157653 ↗

Other SPINAL VERTEBRAL BODY REPLACEMENT DEVICE devices

All SPINAL VERTEBRAL BODY REPLACEMENT DEVICE devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.