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PRO 705461Recalls & reported problems

Stryker GmbH · Jungbluth Clamp · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327131871), received between Jul 30, 2018 and May 26, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

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

  • Break2
  • Fracture1

Patient problems

  • Foreign Body In Patient1
  • Insufficient Information1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 26, 2023Break; Fracture; Break; Fracture

    IT WAS REPORTED THAT THE INSTRUMENT BROKE DURING ORDINARY USE.

    Patient problems: Insufficient Information

    MAUDE report 17010924 ↗
  • MalfunctionJul 30, 2018Break

    PRIMARY PROCEDURE, LEFT ACETABULUM. IT WAS REPORTED THAT DURING THE PROCEDURE, THE CLAMP BROKE AT THE HINGE. THE BROKEN PART WAS EASILY SEEN AND RETRIEVED FROM THE PATIENT. A SURGICAL DELAY OF APPROXIMATELY THREE MINUTES WAS REPORTED.

    Patient problems: Foreign Body In Patient

    MAUDE report 7732837 ↗

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.