Skip to content

C-Taper Head 06-2610Recalls & reported problems

Howmedica Osteonics Corp. · Low Friction Ion Treatment · Class 2 · Implant

All models of C-Taper Head (18)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
1
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327016253), received between Sep 12, 2018 and Sep 12, 2018 — classified as 1 death.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

3 other recalls cover devices cleared under the same FDA submission (K910988, K993601); they may or may not involve this specific model.

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

  • Ambulation or Postural Difficulties1
  • Death1
  • Fatigue1
  • Pain1
  • Rash1
  • Thyroid Problems1
  • Unspecified Infection1

Recent adverse event reports

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

  • DeathSep 12, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

    ITS ALLEGED BY THE PATIENT'S SON, THROUGH THE FILLING OF A LEGAL CLAIM, THAT THE PATIENT UNDERWENT A RIGHT HIP HEMIARTHROPLASTY ON (B)(64) 2014. IT IS FURTHER ALLEGED THAT AFTER IMPLANTATION THE PATIENT EXPERIENCED PAIN, INFECTION, THYROID PROBLEMS, LEG LENGTH DISCREPANCY, WEIGHT GAIN, SKIN RASHES AND FATIGUE. PATIENT SUBSEQUENTLY DIED.

    Patient problems: Ambulation or Postural Difficulties; Death; Fatigue; Pain; Rash; Thyroid Problems; Unspecified Infection

    MAUDE report 7868351 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K910988, K993601. One submission often covers many models, so check the product and lot details in each record.

  • Z-0390-2010 · Sep 4, 2009 · Terminated
    Stryker Howmedica Osteonics, Skirted 5 40' Taper V40 Femoral Head (26 mm +8mm offset), hip prosthesis component.
  • Z-0391-2010 · Sep 4, 2009 · Terminated
    Stryker Howmedica Osteonics, Skirtless 5 40' LFIT V40 Femoral Head (32 mm +0 mm offset); hip prosthesis component.
  • Z-1822-2009 · Jun 18, 2009 · Terminated
    V 40 Femoral Head, Sterile, 22 mm; Catalog number 6260-4-122, Catalog number 6260-5-226; Howmedica Osteonics Corp., Stryker Ireland, Carrigtwohill County Cork, Ireland; Intended f

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

All Prosthesis, hip, semi-constrained, metal/polymer, uncemented devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page