NA 8486621Recalls & reported problems
Richard Wolf GmbH · MINIATURE GRASPING FORCEPS Ø 2MM jaw straight, sheath straight, WL 60mm, reusable · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 04055207017692), received between Mar 5, 2018 and Mar 5, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Bent1
- Material Fragmentation1
Patient problems
- Device Embedded In Tissue or Plaque1
- 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.
MalfunctionMar 5, 2018Bent; Material Fragmentation; Bent; Material Fragmentation
RICHARD WOLF (B)(4) WAS INFORMED BY THE USER FACILITY THAT GRASPING FORCEPS (ID #8486.21) BROKE DURING USE AND THE JAW PART OF THE DEVICE STILL REMAINS IN THE PATIENT'S CARPUS. USER FACILITY EMAILED AND CALLED TO REQUEST MISSING/ADDITIONAL INFORMATION, NO RESPONSE AS OF 05MAR2018. MANUFACTURED DATE: 28APR2009, LOT SIZE: (B)(4) UNITS, PURCHASE DATE: 10AUG2009.
Patient problems: Device Embedded In Tissue or Plaque; Foreign Body In Patient
MAUDE report 7314369 ↗
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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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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