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Anato 4845-7-113Recalls & reported problems

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

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 07613252631149), received between Oct 2, 2018 and Oct 2, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • Bone Fracture(s)1
  • Injury1

Recent adverse event reports

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

  • InjuryOct 2, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

    AS REPORTED: "PATIENT PRESENTED TO E.R. WITH PAINFUL HIP AFTER FALL. X-RAY REVEALED PERI-PROSTHETIC FRACTURE...REVISED WITH OMNIFIT EON STEM".

    Patient problems: Bone Fracture(s); Injury

    MAUDE report 7927377 ↗

Other Prosthesis, hip, semi-constrained, metal/polymer, uncemented 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.