RINGLOC + HIP SYSTEM 106024Recalls & reported problems
Biomet Orthopedics, LLC · Class 2 · Implant
All models of RingLoc Hip System (40)
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 00880304455078), received between Jan 20, 2020 and Jan 20, 2020 — classified as 1 injury.
19 other recalls cover devices cleared under the same FDA submission (K070369); 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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Extraskeletal ossification1
- Pain1
- Scar Tissue1
- Unspecified Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
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 9608261 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K070369. One submission often covers many models, so check the product and lot details in each record.
- Z-2463-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Limited Hole Acetablular Cup, 52 mm Size 23, with Locking Ring, sterile, REF PT-116052, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ringl
- Z-2452-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Solid Acetablular Cup w/Apical Hole, 64 mm Size 26, w/Lock Ring w/Plug, sterile, REF PT-104064, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenere
- Z-2465-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Limited Hole Acetablular Cup, 56 mm Size 24, with Locking Ring, sterile, REF PT-116056, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ring
- Z-2466-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Limited Hole Acetablular Cup, 60 mm Size 25, with Locking Ring, sterile, REF PT-116060, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ring
- Z-2462-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Limited Hole Acetablular Cup, 50 mm Size 22, with Locking Ring, sterile, REF PT-116050, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ringl
- Z-2464-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Limited Hole Acetablular Cup, 54 mm Size 23, with Locking Ring, sterile, REF PT-116054, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ring
- Z-2454-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Multi Hole Acetablular Cup, 56 mm Size 24, with Lock Ring, sterile, REF PT-106056, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ringloc is
- Z-2456-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Multi Hole Acetablular Cup, 62 mm Size 25, with Lock Ring, sterile, REF PT-106062, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ringloc is
- Z-2459-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Multi Hole Acetablular Cup, 70 mm Size 27, with Lock Ring, sterile, REF PT-106070, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ringloc is
- Z-2460-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Multi Hole Acetablular Cup, 74 mm Size 28, with Lock Ring, sterile, REF PT-106074, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ringloc is
- Z-2450-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Solid Acetablular Cup w/Apical Hole, 56 mm Size 24, w/Lock Ring w/Plug, sterile, REF PT-104056, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenere
- Z-2461-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Limited Hole Acetablular Cup, 48 mm Size 22, with Locking Ring, sterile, REF PT-116048, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ring
- Z-2448-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Solid Acetablular Cup w/Apical Hole, 50 mm Size 22, w/Lock Ring w/Plug, sterile, REF PT-104050, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous
- Z-2455-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Multi Hole Acetablular Cup, 60 mm Size 25, with Lock Ring, sterile, REF PT-106060, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ringloc is
- Z-2457-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Multi Hole Acetablular Cup, 64 mm Size 25, with Lock Ring, sterile, REF PT-106064, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ringloc is
…and 4 more.
Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices
- BIOLOX DELTA 1365-32-310Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented551 reports
- PINNACLE ALTRX 1221-36-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented481 reports
- BIOLOX DELTA 1365-32-320Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death314 reports
- BIOLOX DELTA 1365-36-720Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death189 reports
- DJO SURGICAL 400-03-362Encore Medical, L.P. · Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented187 reports
- Anthology 71365705Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented176 reports
- BIOLOX DELTA 1365-40-710Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented170 reports
- PINNACLE GRIPTION 1217-32-054Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented169 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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