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UNIVERSAL NEURO 2, UNIVERSAL NEURO III 54-00647Recalls & reported problems

Stryker Leibinger GmbH & Co. KG · DYNAMIC MESH STD F. 1.5/1.7MM SCREWS · 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 04546540237668), received between Sep 8, 2022 and Sep 8, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • InjurySep 8, 2022Fracture; Fracture

    IT WAS REPORTED THAT MESH HAD BEEN IMPLANTED FOR 16 YEARS AND RECENTLY, IT WAS FOUND THAT IT WAS BROKEN. THERE WAS A REVISION SURGERY PERFORMED TO REMOVE THE MESH.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15382240 ↗

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Sources and updates

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