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Citation 6265-5218Recalls & reported problems

Howmedica Osteonics Corp. · 132 Degree Neck Angle V40 Hip Stem - Right · Class 2 · Implant

All models of Citation (20)

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 07613154316113), received between Nov 19, 2021 and Nov 19, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1

Patient problems

  • Ambulation or Postural Difficulties1
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • InjuryNov 19, 2021Fracture; Fracture

    IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED DUE TO THE TRUNNION OF THE CITATION STEM BREAKING OFF. SURGEON REPORTED PATIENT IS VERY ACTIVE, CYCLING 30 MILES PER DAY. THE STEM AND HEAD WERE REVISED. THERE ARE NO ALLEGATIONS AGAINST THE REVISED HEAD.

    Patient problems: Ambulation or Postural Difficulties; No Clinical Signs, Symptoms or Conditions

    MAUDE report 12844036 ↗

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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