REVISION REVISION HIP - Ti6Al4V (REF 7515.15.040)Recalls & reported problems
Limacorporate SPA · Neck with Screw H=90mm Taper 12/14 · 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 08033390017770), received between Jan 26, 2026 and Jan 26, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).
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
- Device Dislodged or Dislocated1
Patient problems
- Joint Dislocation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 26, 2026Device Dislodged or Dislocated
REVISION SURGERY WAS PERFORMED ON (B)(6) 2025 DUE TO DISLOCATION OF HIP PROSTHESIS. PREVIOUS SURGERY OCCURRED ON (B)(6) 2025 AND TRACED IN ANOTHER COMPLAINT (REPORTED AS MFR. 3008021110-2026-00049). PATIENT DISLOCATED THE HIP PROSTHESIS CONSISTING OF: REVISION MODULAR NECK H.90MM (PART NUMBER 7515.15.040, LOT 2124174, STERILIZATION (B)(4), MOBILE LINER ØINT 28 MM Ø42 MM (PART NUMBER 5566.50.420, LOT 25AT0X1, STERILIZATION (B)(4), FEM. MODULAR HEAD - XL Ø28MM (PART NUMBER 5010.09.284, LOT 2436599, STERILIZATION (B)(4). THE REVISION NECK WAS REPLACED WITH ANOTHER ONE AND THE LINER WAS REMOVED TO IMPLANT A COSTRAINED LINER FROM ANOTHER MANUFACTURER. SURGERY WAS COMPLETED AS INTENDED. PATIENT IS FEMALE, DATE OF BIRTH (B)(6) 1942. THE EVENT OCCURRED IN THE UNITED STATES.
Patient problems: Joint Dislocation
MAUDE report 24176873 ↗
Other Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented devices
- STAGEONE 431209Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented2 recalls0 reports
- SELF CENTERING 1035-45-000Depuy Orthopaedics, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented84 reports
- LFIT 6260-9-036Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented80 reports
- ACTIS 101011060Depuy (Ireland) · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented66 reports
- RINGLOC BI-POLAR HIP SYSTEM 11-165228Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall1 death12 reports
- SELF CENTERING 1035-44-000Depuy Orthopaedics, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented60 reports
- TANDEM 71324046Smith & Nephew, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall9 reports
- TAPERLOC COMPLETE XR 123 MICRO FEMORAL 51-145170Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented59 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.
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