NA NNR-0FRecalls & reported problems
Fehling Instruments GmbH & Co. KG · CERAMO punch w. ejec. flatfoot filigree, 40° upw., 2.0x200mm · Class 2
- 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 04058749063394), received between Mar 3, 2022 and Mar 3, 2022 — classified as 1 malfunction.
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. How this data works · Data updated Oct 13, 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.
MalfunctionMar 3, 2022Fracture; Fracture
A CERVICAL KERRISION BROKE DURING THE PROCEDURE WHILE IN USE. ALL PIECES WER RETRIEVED BY THE SURGEON.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13657803 ↗
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- Symmetry Rapidclean® 53-1624LDAspen Surgical Products, Inc. · Rongeur, Manual2 reports
- V. Mueller NL4291-81TSteris Corporation · RONGEUR, MANUAL2 reports
- V. Mueller NL6147Steris Corporation · RONGEUR, MANUAL2 reports
- Millennium 85-2481559Avalign Technologies, Inc. · RONGEUR, MANUAL1 report
- Symmetry KERRISON 53-1405Aspen Surgical Products, Inc. · Rongeur, Manual1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.