Regenerex® Ringloc®+ Hip System PT-106068Recalls & reported problems
Biomet Orthopedics, LLC · Class 2 · Implant
Data updated Oct 18, 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 00887868341977), received between Jun 2, 2026 and Jun 2, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Malposition of Device” (1 report).
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Malposition of Device1
Patient problems
- Joint Dislocation1
- Radiolucent Lines1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 2, 2026Malposition of Device
IT WAS REPORTED THE PATIENT UNDERWENT A SECOND LEFT TOTAL HIP REVISION APPROXIMATELY 2 YEARS AND 2 MONTHS AFTER A PRIOR REVISION DUE TO RECURRENT POSTERIOR DISLOCATIONS. THE PATIENT PREVIOUSLY UNDERWENT AN INITIAL LEFT TOTAL HIP ARTHROPLASTY, AND APPROXIMATELY 7 YEARS POST-IMPLANTATION WAS REVISED DUE TO PAIN, METALLOSIS, AND OSTEOLYSIS. DURING THE SECOND REVISION, INTRA-OPERATIVE FINDINGS INCLUDED LUCENCY OF THE ACETABULAR CUP, TWO FRACTURED ACETABULAR SCREWS, AND THE CUP POSITIONED IN RETROVERSION. ALL IMPLANTS EXCEPT THE FEMORAL STEM WERE REVISED WITHOUT COMPLICATION. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Joint Dislocation; Radiolucent Lines
MAUDE report 25361445 ↗
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-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-2451-2011 · Apr 14, 2011 · TerminatedRegenerex (TM) Ringloc +, Solid Acetablular Cup w/Apical Hole, 62 mm Size 25, w/Lock Ring w/Plug, sterile, REF PT-104062, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenere
- 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-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-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-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-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
- 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-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-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-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-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-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-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
…and 4 more.
Other Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate devices
- Novation 130-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls156 reports
- Novation 130-36-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls79 reports
- CORAIL 3L92511Depuy (Ireland) · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate158 reports
- Acumatch A Series 138-36-29Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate3 recalls1 report
- Novation 136-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls43 reports
- Novation 130-32-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls33 reports
- Novation 132-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls26 reports
- Novation 136-36-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls22 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page