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Hip Instruments 01.18.10.207Recalls & reported problems

Medacta International SA · AMIStem Broach # 7 - Dr. Jackob · Class 1

All models of Hip Instruments (48)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 07630040752053), received between Dec 18, 2018 and Dec 18, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Fracture1

Patient problems

  • Bone Fracture(s)1

Recent adverse event reports

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

  • InjuryDec 18, 2018Fracture

    DURING THE PRIMARY HIP SURGERY, WHILE BROACHING THE FEMUR IN ORDER TO IMPLANT THE STEM, THE FEMUR FRACTURED. THIS "CASUED" A 10 MINUTE DELAY IN THE CASE AND THE SURGEON WAS ABLE TO CABLE THE FRACTURE. THE REPORTER STATED HE WAS NOT CERTAIN ON REASON FOR FRACTURE, BUT IT OCCURRED WHILE BROACHING WITH THE #7 BROACH. TYPE B FEMUR; NOT CERTAIN ON PATIENT BONE QUALITY.

    Patient problems: Bone Fracture(s)

    MAUDE report 8173611 ↗

Other Orthopedic Manual Surgical Instrument devices

All Orthopedic Manual Surgical Instrument devices →

Sources and updates

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