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TRI-LOCK GRIPTION 1012-04-120Recalls & reported problems

Depuy Orthopaedics, Inc. · TRI-LOCK BPS FEMORAL STEM 12/14 TAPER TRI-LOCK BPS W/GRIPTION SIZE 12 STD 119mm · Class 3 · Implant

All models of TRI-LOCK GRIPTION (26)

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 10603295000839), received between Aug 24, 2018 and Aug 24, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 16, 2026.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • Bone Fracture(s)1
  • Not Applicable1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryAug 24, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

    IT WAS REPORTED THAT POST OP X-RAYS REVEALED THE FEMUR FRACTURED. UNCLEAR WHEN THE FRACTURE OCCURRED. THE COMPONENTS WERE REMOVED AND CONVERTED TO A TOTAL HIP REPLACEMENT WITH ORIF. DOI: (B)(6) 2018. DOR: (B)(6) 2018. LEFT HIP.

    Patient problems: Bone Fracture(s); Not Applicable

    MAUDE report 7812466 ↗

Other Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented devices

All Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented devices →

Sources and updates

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