Secur-Fit S-2337-HF06Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327020571), received between Apr 5, 2021 and Apr 5, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Migration or Expulsion of Device” (1 report).

1 other recall cover devices cleared under the same FDA submission (K941366); 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 18, 2026.

Most reported problems

Recent adverse event reports

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

• InjuryApr 5, 2021Migration or Expulsion of Device; Osseointegration Problem; Migration or Expulsion of Device; Osseointegration Problem

  IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED DUE TO LOOSENING OF THE FEMORAL STEM. THE STEM, 22 +5 C-TAPER HEAD, AND 36C ADM/ MDM POLY WERE REVISED TO A RESTORATION MODULAR STEM CONSTRUCT, 22 +0 V40 HEAD, AND ANOTHER 36C ADM/ MDM POLY. REP PROVIDED AN X-RAY. REP ALSO CONFIRMED THERE ARE NO ALLEGATIONS AGAINST THE REVISED HEAD AND LINER, AND THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Insufficient Information; Pain

  MAUDE report 11616065 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K941366. One submission often covers many models, so check the product and lot details in each record.

• Z-0902-2009 · Nov 13, 2008 · Terminated
  Secur-Fit ARC/HA Collar Stem These devices are modular components of a total hip system. These femoral stems are intended for use with femoral heads and acetabular components in p