Secur-Fit 6052-0730SRecalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 07613327021103), received between Mar 9, 2018 and Dec 22, 2023 — classified as 6 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (4 reports).

2 other recalls cover devices cleared under the same FDA submission (K041170, K051738); 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 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryDec 22, 2023Loss of Osseointegration; Migration; Loss of Osseointegration; Migration

  PATIENT UNDERWENT LEFT TOTAL HIP ARTHROPLASTY ON (B)(6) 2014 SUBSEQUENTLY HE DEVELOPED SEVERE THIGH PAIN, PAIN ON WEIGHTBEARING AND PAIN AT NIGHT. X-RAYS ALLEGEDLY DEMONSTRATED SETTLING OF HIS PROSTHESIS. HE WAS REVISED ON MAY 8, 2015 DUE TO ALLEGED LOOSENING OF HIS LEFT FEMORAL HIP COMPONENT.

  Patient problems: Inadequate Osseointegration; Pain

  MAUDE report 18382235 ↗
• InjuryApr 15, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THROUGH THE SUBMISSION OF A REVISION IMPLANT SHEET THAT THE PATIENT'S RIGHT HIP WAS REVISED. THE SALES BRANCH PROVIDED THE PRIMARY AND REVISION USAGE SHEETS. A SECUR-FIT MAX STEM, BIOLOX CERAMIC HEAD, AND X3 ELEVATED RIM INSERT WERE REVISED TO A RESTORATION MODULAR STEM CONSTRUCT, 28 +4 CERAMIC HEAD, MDM LINER WITH ADM/MDM INSERT, AND 4 SETS OF DALL-MILES CABLES. UPDATE: "PATIENT SUFFERED PERIPROSTHETIC HIP FRACTURE FOLLOWING A FALL."

  Patient problems: Bone Fracture(s); Injury

  MAUDE report 9963630 ↗
• InjuryJan 9, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT HAD PERIPROSTHETIC FRACTURE OF LEFT HIP FROM PREVIOUS TOTAL HIP DONE ON (B)(6) 2006. UPDATE: "LEFT HIP PROXIMAL FEMUR WAS FRACTURED STEM REMOVED , HEAD REMOVED POLY WAS EXCHANGED."

  Patient problems: Hip Fracture; Injury

  MAUDE report 9568220 ↗
• InjuryJan 4, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT HAD A PRIMARY TOTAL HIP (B)(6) 2018. SHE FELL IN REHAB AND FRACTURED HER FEMUR. SHE WAS TAKEN TO THE OPERATING ROOM AND REVISED TO A CONE CONICAL WITH A DALL MILES TROCHANTERIC PLATE AND CABLES. OPERATION WAS COMPLETED SUCCESSFULLY.

  Patient problems: Bone Fracture(s); Injury

  MAUDE report 8217974 ↗
• InjuryDec 4, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT HAD A PRIMARY TOTAL HIP. SHE DID WELL UNTIL SHE FELL. SHE WAS SEEN IN THE ER AND X-RAYS WERE TAKEN. SHE SUSTAINED A PERIPROSTHETIC FRACTURE. SHE WAS TAKEN TO THE OR AND REVISED.

  Patient problems: Bone Fracture(s); Fall; Injury

  MAUDE report 8130282 ↗
• InjuryMar 9, 2018Migration or Expulsion of Device; Migration or Expulsion of Device

  AS REPORTED: "SUBSIDED FEMORAL STEM. RE-IMPLANTED WITH NEW STEM."

  Patient problems: Injury

  MAUDE report 7326502 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K041170, K051738. One submission often covers many models, so check the product and lot details in each record.

• Z-0894-2009 · Nov 13, 2008 · Terminated
  Primary Secur-fit Plus Max Hip Stem These devices are modular components of a total hip system. These femoral stems are intended for use with femoral heads and acetabular componen
• Z-0893-2009 · Nov 13, 2008 · Terminated
  Secur-Fit Max Hip 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 primary