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RESORB X, STERILE 52-310-31-04Recalls & reported problems

KLS-Martin L.P. · MESH, SMALL GRID, PDLLA · Class 2 · Implant

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 00888118000811), received between Jul 30, 2018 and Jul 30, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (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

  • Material Fragmentation1

Patient problems

  • Hydrocephalus1
  • Impaired Healing1
  • Wound Dehiscence1

Recent adverse event reports

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

  • InjuryJul 30, 2018Material Fragmentation; Material Fragmentation

    IT WAS REPORTED DUE TO PATIENT COMPLICATIONS THE RESORB X FRAGMENTED AND HAD TO BE REMOVED.

    Patient problems: Hydrocephalus; Impaired Healing; Wound Dehiscence

    MAUDE report 7732794 ↗

Other PLATE, BONE devices

All PLATE, BONE devices →

Sources and updates

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