RingLoc+ Hip System 16-104160Recalls & 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 00880304592933), received between Nov 2, 2021 and Nov 2, 2021 — classified as 1 injury.
30 other recalls cover devices cleared under the same FDA submission (K093235); 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
- Ambulation or Postural Difficulties1
- Metal Related Pathology1
- Necrosis1
- Pain1
- Swelling/ Edema1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 2, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Ambulation or Postural Difficulties; Metal Related Pathology; Necrosis; Pain; Swelling/ Edema
MAUDE report 12738762 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K093235. One submission often covers many models, so check the product and lot details in each record.
- Z-0312-2018 · Jun 29, 2017 · TerminatedPPS RingLoc+ Acetabular Shell, RNGLC+ LTD HOLE SHELL SZ62 The Porous Plasma Spray (PPS) Ringloc+ Acetabular System is intended to replace the natural acetabulurn damaged by disea
- Z-2483-2015 · Jul 28, 2015 · TerminatedVision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.
- Z-1123-2015 · Jan 9, 2015 · TerminatedRingloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component.
- Z-2432-2011 · Apr 14, 2011 · TerminatedRingloc + Acetabular Shell limited hole finned 70 mm Size 28 porous coat, for uncemented use, sterile, REF 16-104170, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plas
- Z-2434-2011 · Apr 14, 2011 · TerminatedRingloc + Acetabular Shell limited hole, 48 mm Size 22, porous coat, for uncemented use, sterile, REF 16-116048, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plasma Sp
- Z-2421-2011 · Apr 14, 2011 · TerminatedRingloc + Acetabular Shell limited hole finned 46 mm Size 22 porous coat, for uncemented use, sterile, REF 16-104146, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plas
- Z-2431-2011 · Apr 14, 2011 · TerminatedRingloc + Acetabular Shell limited hole finned 66 mm Size 27 porous coat, for uncemented use, sterile, REF 16-104166, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plas
- Z-2439-2011 · Apr 14, 2011 · TerminatedRingloc + Acetabular Shell limited hole, 58 mm Size 25, porous coat, for uncemented use, sterile, REF 16-116058, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plasma Sp
- Z-2426-2011 · Apr 14, 2011 · TerminatedRingloc + Acetabular Shell limited hole finned 56 mm Size 24 porous coat, for uncemented use, sterile, REF 16-104156, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plas
- Z-2444-2011 · Apr 14, 2011 · TerminatedRingloc + Acetabular Shell limited hole, 68 mm Size 27, porous coat, for uncemented use, sterile, REF 16-116068, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plasma Sp
- Z-2443-2011 · Apr 14, 2011 · TerminatedRingloc + Acetabular Shell limited hole, 66 mm Size 27, porous coat, for uncemented use, sterile, REF 16-116066, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plasma Sp
- Z-2436-2011 · Apr 14, 2011 · TerminatedRingloc + Acetabular Shell limited hole, 52 mm Size 23, porous coat, for uncemented use, sterile, REF 16-116052, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plasma Sp
- Z-2429-2011 · Apr 14, 2011 · TerminatedRingloc + Acetabular Shell limited hole finned 62 mm Size 26 porous coat, for uncemented use, sterile, REF 16-104162, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plas
- Z-2430-2011 · Apr 14, 2011 · TerminatedRingloc + Acetabular Shell limited hole finned 64 mm Size 26 porous coat, for uncemented use, sterile, REF 16-104164, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plas
- Z-2441-2011 · Apr 14, 2011 · TerminatedRingloc + Acetabular Shell limited hole, 62 mm Size 26, porous coat, for uncemented use, sterile, REF 16-116062, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plasma Sp
…and 15 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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