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AESCULAP MB510Recalls & reported problems

Aesculap, Inc. · Blade Clamp, tilting, non-sterile, reusable · Class 1

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 04046964567568), received between Jul 14, 2021 and Jul 14, 2021 — classified as 1 injury.

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

Most reported problems

Device problems

  • Fitting Problem1

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.

  • InjuryJul 14, 2021Fitting Problem; Fitting Problem

    ASSOCIATED MEDWATCHES: 2916714-2021-00143.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12166897 ↗

Other RETRACTOR devices

All RETRACTOR devices →

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