Skip to content

FIREBIRD SFS 51-7111Recalls & reported problems

Orthofix US LLC · HOOK PUSHER · 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 18257200046560), received between May 17, 2017 and May 17, 2017 — 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
  • Difficult to Open or Close1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionMay 17, 2017Device Slipped; Difficult to Open or Close

    INFORMATION PROVIDED STATES THAT WHILE TRYING TO INSERT LUMBAR LAMINA HOOKS, SURGEON STATED HOOK KEPT FALLING OFF. UPON INSPECTION BOTH HOOK PUSHERS WERE FAILING TO CLOSE ALL THE WAY RESULTING IN A DELAY IN THE CASE. THERE WERE NO ADVERSE EFFECTS TO THE PATIENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 6572119 ↗

Other PUSHER, SOCKET devices

All PUSHER, SOCKET devices →

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