NA COD-1TRecalls & reported problems
Fehling Instruments GmbH & Co. KG · CERAMO RONDO TORLOCK non-traum.micro forceps, 1.2 x 180 mm · 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 04058749121391), received between Mar 17, 2026 and Mar 17, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Material Deformation” (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.
Reports received per month
Most reported problems
Device problems
- Material Deformation1
Patient problems
- Intraoperative Cardiac Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 17, 2026Material Deformation
THIS IS A FINE MICRO-FORCEPS USED IN SURGERY. THE TEETH OF THE WORKING PART AT THE DISTAL END ARE DAMAGED. THE LAST TOOTH OF THE SINGLE ROW OF TEETH IS BENT DISTALLY AND PARTIALLY TORN AWAY FROM THE BASE MATERIAL. FURTHERMORE, THE SURFACE OF THE TEETH AT THE AFFECTED POINT IS PARTIALLY DEFORMED AND EXPOSED BARE METAL. INTRAOPERATIVE FINDING: UPON PALPATION OF THE HEART MUSCLE, A TEAR IN THE TISSUE WITH BLEEDING OCCURRED. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: Intraoperative Cardiac Injury
MAUDE report 24617402 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.