RingLoc® Hip System 103532Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00880304008694), received between Jan 20, 2020 and Nov 12, 2025 — classified as 2 injuries.

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

5 other recalls cover devices cleared under the same FDA submission (K082446, K912245, K971890, K990032, K991807); 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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryNov 12, 2025Migration; Migration

  IT WAS REPORTED THAT THE PATIENT IS BEING CONSIDERED FOR A RIGHT HIP REVISION. THE PATIENT FELL AND DISASSOCIATED THE IMPLANT FROM THE PELVIS. THE TRIFLANGE SCREWS HAD STARTED TO RIP OUT FROM THE PELVIS FOLLOWING THE FALL. NO KNOWN REVISION HAS TAKEN PLACE. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Joint Dislocation

  MAUDE report 23534303 ↗
• InjuryJan 20, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT UNDERWENT RIGHT REVISION AND SUBSEQUENTLY, PATIENT UNDERWENT ANOTHER REVISION A YEAR AND A HALF LATER DUE TO INFECTION. ALL COMPONENTS WERE REMOVED AND A CEMENT SPACER IMPLANTED. ATTEMPTS WERE MADE TO OBTAIN ADDITIONAL INFORMATION; HOWEVER, NONE WAS AVAILABLE.

  Patient problems: Extraskeletal ossification; Pain; Scar Tissue; Unspecified Infection

  MAUDE report 9608259 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K082446, K912245, K971890, K990032, K991807. One submission often covers many models, so check the product and lot details in each record.

• Z-0627-2021 · Nov 25, 2020 · Terminated
  RINGLOC ACETABULAR SYSTEM Self-tapping bone screws, Item numbers 103531, 103533, 103534, 103535 - Product Usage: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented; Prosthe
• Z-0621-2021 · Nov 25, 2020 · Terminated
  Custom Cancellous Thread, Item numbers CP161941, CP161943 - Product Usage: 1. Noninflammatory degenerative joint disease including osteoarthritis and avascular necrosis. 2. Rheu
• Z-1086-2019 · Mar 1, 2019 · Terminated
  Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx20mm-Low Profile Titanium. Accessory to total hip implant Item Number: 103531 Product Usage: Accessory to total hip implant
• Z-1087-2019 · Mar 1, 2019 · Terminated
  Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx30mm-Low Profile Titanium, Accessory to total hip implant Item Number: 103533 Product Usage: Accessory to total hip implant
• Z-2135-2011 · Mar 10, 2011 · Terminated
  Low Profile Self-Tapping Bone Screw, 6.5 mm X 25 mm, Qty. 1, Biomet Orthopedics, 66 East Bell Drive, P.O. Box 587, Warsaw, IN 46581 USA. STERILE. To provide fixation of any acetab