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Anato 4845-7-214Recalls & reported problems

Howmedica Osteonics Corp. · NEUTRAL 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 07613252631316), received between Jul 3, 2019 and Jul 3, 2019 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.

  • InjuryJul 3, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

    THIS PI IS FOR THE REVISED IMPLANTS OF THE LEFT HIP. IT WAS REPORTED THAT THE PATIENT SUFFERED BILATERAL FEMORAL FRACTURES 6 DAYS AFTER HAVING A BILATERAL HIP REPLACEMENT. THE ANATO STEMS AND BIOLOX HEADS WERE REVISED TO RESTORATION MODULAR STEM CONSTRUCTS AND BIOLOX HEADS.

    Patient problems: Bone Fracture(s); Injury

    MAUDE report 8758220 ↗

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

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

Sources and updates

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