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PRO 705464Recalls & reported problems

Stryker GmbH · Farabeuf Clamp · Class 1

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 07613327131901), received between Jul 12, 2021 and Jul 12, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Slipped” (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

  • Device Slipped1
  • Positioning Failure1

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.

  • MalfunctionJul 12, 2021Positioning Failure; Device Slipped; Positioning Failure; Device Slipped

    AS REPORTED: "THE PHYSICIAN WAS ATTEMPTING TO REDUCE THE PELVIC WING TO THE SACRUM USING THE FARABEUF CLAMP. THE CLAMP CONTINUALLY SLIPPED AND WOULDN¿T LOCK PROPERLY. THE PHYSICIAN USED BOTH THE ANGLED AND THE STRAIGHT FARABEUF CLAMP DURING THE SURGERY BUT BOTH OF THEM KEPT COMING UNDONE. THESE CLAMPS ARE SUPPOSED TO STAY LOCKED ONCE THEY ARE POSITIONED."ADDITIONAL INFORMATION: PROCEDURE WAS COMPLETED USING SYNTHES CLAMPS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12150154 ↗

Other CLAMP devices

All CLAMP devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.