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n/a 610-0010Recalls & reported problems

Ortho Development Corporation · Broach Size 10 · Class 1

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 00822409088751), received between Oct 23, 2020 and Oct 23, 2020 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Hip Fracture1

Recent adverse event reports

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

  • InjuryOct 23, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    DURING TOTAL HIP ARTHROPLASTY, AN INTRAOPERATIVE FRACTURE OF THE GREATER TROCHANTER OCCURRED DURING BROACHING. THE SURGEON REINFORCED THE FRACTURE WITH CABLE. THE SURGEON COMMENTED THAT THE PATIENT'S FRAGILE BONE QUALITY WAS THE CAUSE.

    Patient problems: Hip Fracture

    MAUDE report 10731349 ↗

Other ORTHOPEDIC MANUAL SURGICAL INSTRUMENT devices

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