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MODULIFT MF655TRecalls & reported problems

Aesculap AG · MODULIFT VBR SZ.M MODULAR 30-40MM · Class 2 · Implant

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 04046964022395), received between Mar 23, 2021 and Mar 23, 2021 — classified as 1 malfunction.

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

  • Degraded1
  • Difficult to Remove1

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.

  • MalfunctionMar 23, 2021Degraded; Difficult to Remove; Degraded; Difficult to Remove

    CLARIFICATION: THE PROCEDURE WAS A VERTEBRAL BODY REPLACEMENT (VBR). THE SURGEON HAD ASKED FOR A CHANGE IN THE END CAP ANGLES.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11553801 ↗

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