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AMIStem-H Proximal Coating Femoral Stems 01.18.186Recalls & reported problems

Medacta International SA · AMIStem-H Proximal Coating Lat. #6 · Class 2 · Implant

All models of AMIStem-H Proximal Coating Femoral Stems (11)

Data updated Oct 18, 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 07630030804519), received between May 27, 2021 and May 27, 2021 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Unequal Limb Length1

Recent adverse event reports

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

  • InjuryMay 27, 2021Appropriate Device Problem Term/Code Not Available

    REVISION SURGERY PERFORMED 6 WEEKS AFTER THE PRIMARY SURGERY ON (B)(6) 2021 DUE TO LEG LENGTH DISCREPANCY (THE LEG WAS 3 CM LONGER). ALL IMPLANTS REVISED. LOT NUMBERS AND PRIMARY DATE ARE UNAVAILABLE.

    Patient problems: Unequal Limb Length

    MAUDE report 11893149 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented devices

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Sources and updates

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