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AMIStem-P Short Neck 01.18.464Recalls & reported problems

Medacta International SA · AMIStem-P Short Neck STD stem #4 · Class 2 · Implant

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 07630971243682), received between Aug 23, 2021 and Aug 23, 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

  • Adverse Event Without Identified Device or Use Problem1

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.

  • InjuryAug 23, 2021Adverse Event Without Identified Device or Use Problem

    OBLIQUE BONE FRACTURE AROUND THE TIP OF THE FEMORAL STEM WAS REPORTED. THE FRACTURE LED TO STEM SUBSIDENCE. THE SUBSIDENCE WAS OBSERVED ABOUT 2-3 WEEKS AFTER THE PRIMARY SURGERY. THE BONE WAS FIXED WITH A PLATE. NO IMPLANTS WERE REVISED. ADDITIONAL SURGERY DATE IS UNKNOWN.

    Patient problems: Bone Fracture(s)

    MAUDE report 12352936 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented devices

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Sources and updates

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