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JAZZ System JAZZ Claw – Hook LeftRecalls & reported problems

Implanet · Hook Left · Class 2

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 03607503507127), received between Jun 12, 2017 and Jun 12, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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

  • Improper or Incorrect Procedure or Method1

Patient problems

  • Patient Problem/Medical Problem1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 12, 2017Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method

    IMPLANTABLE HARDWARE DISLODGED IN SITU DUE TO PATIENT PATHOLOGY PROGRESSION. PRODUCTS REMOVED DURING REVISION SURGERY 4 WEEKS POST SURGERY. ALTERNATIVE IMPLANTABLE USED TO REPLACE.

    Patient problems: Patient Problem/Medical Problem

    MAUDE report 6633200 ↗

Other Bone Fixation Cerclage, Sublaminar devices

All Bone Fixation Cerclage, Sublaminar devices →

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