ERAGON MODULAR 8395214Recalls & reported problems
Richard Wolf GmbH · BABCOCK FORCEPS INSERT Ø 10MM jaw length 38mm, for SL 327mm, double action, 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 04055207016756), received between Aug 13, 2025 and Aug 13, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Material Fragmentation” (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 Fragmentation1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 13, 2025Material Fragmentation; Material Fragmentation
IT WAS REPORTED THAT DURING A LAPAROSCOPIC CHOLECYSTECTOMY, THE JOINT HINGE OF ONE ARM OF THE BABCOCK FORCEPS BROKE OFF. IT FELL INTO THE SURGICAL SITE AND COULD NOT BE RETRIEVED EVEN WITH THE AID OF A C-ARM MACHINE. THE SURGERY WAS EXTENDED BY APPROXIMATELY AN HOUR.
Patient problems: Foreign Body In Patient
MAUDE report 22798076 ↗
Other FORCEPS, GENERAL & PLASTIC SURGERY devices
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- Centurion 66790Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY2 recalls0 reports
- Sklar Instruments 96-2549Sklar Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall2 reports
- Centurion I68420Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall2 reports
- Centurion 66195Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 report
- Centurion 66440Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 report
- Centurion TRI66875Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.