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AESCULAP FF806RRecalls & reported problems

Aesculap AG · LOVE-GRUENWALD Rongeur, 150 °, upwards cutting, 7" (180 mm), 3 x 10 mm · Class 1

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 04038653044603), received between Mar 9, 2021 and Mar 9, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Twisted/Bent” (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

  • Material Twisted/Bent1

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 9, 2021Material Twisted/Bent; Material Twisted/Bent

    ASSOCIATED MEDWATCH-REPORTS: 9610612-2021-00151 ((B)(6) +FF805R) AND 9610612-2021-00152 ((B)(6) +FF806R).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11445680 ↗

Other RONGEUR devices

All RONGEUR devices →

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