ERAGON MODULAR 8393185Recalls & reported problems
Richard Wolf GmbH · GRASP. FORCEPS INSERT Ø 5MM single fenestration with cross toothing, jaw length 21mm, for SL 330mm, single action, reusable · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 04055207015827), received between Jun 24, 2026 and Jun 24, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information1
Patient problems
- Bowel Perforation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 24, 2026Insufficient Device Problem Information
ACCORDING TO THE REPORT, THE FORCEPS HAVE CAUSED TRAUMATIC LESIONS, SOME OF WHICH WITH TRANSMURAL PERFORATION. PATIENT REQUIRING SURGICAL RE-INTERVENTION DUE TO SMALL BOWEL PERFORATIONS. THE USER DID NOT SPECIFY WHETHER A MALFUNCTION OCCURRED WHILE THE FORCEPS WERE BEING USED OR EXACTLY WHAT CIRCUMSTANCES LED TO THE PATIENT'S INJURY.
Patient problems: Bowel Perforation
MAUDE report 25607345 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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