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Anato 4845-7-105Recalls & reported problems

Howmedica Osteonics Corp. · ANTEVERTED 130 Degree Neck Angle V40 Hip Stem · Class 2 · Implant

All models of Anato (13)

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 07613252631088), received between Jul 30, 2021 and Jul 30, 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 16, 2026.

Most reported problems

Device problems

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • InjuryJul 30, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    AS REPORTED: "REVISION SURGERY...EXPLANTED THE ANATO STEM, 36 V40 -2.5 HEAD AND 36F 10° LINER. NO MORE INFORMATION AVAILABLE." SPOKE TO REP. SURGEON REPORTED THAT THE PATIENT'S STEM HAD SUBSIDED. THERE WERE NO ALLEGATIONS AGAINST THE REVISED HEAD OR LINER. REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

    Patient problems: Failure of Implant

    MAUDE report 12252143 ↗

Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish devices

All Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish devices →

Sources and updates

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