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TRI-LOCK GRIPTION 1012-04-110Recalls & reported problems

Depuy Orthopaedics, Inc. · TRI-LOCK BPS FEMORAL STEM 12/14 TAPER TRI-LOCK BPS W/GRIPTION SIZE 11 STD 117mm · 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 10603295000822), received between Aug 16, 2018 and Aug 16, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Malposition of Device” (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

  • Malposition of Device1

Patient problems

  • Pain1

Recent adverse event reports

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

  • InjuryAug 16, 2018Malposition of Device; Malposition of Device

    IT WAS REPORTED THAT VALGUS ALIGNMENT OF TRILOCK STEM COUPLED WITH PATIENT PAIN THAT LED SURGEONS DECISION TO REPLACE FEMORAL COMPONENT. ALSO ECCENTRIC ALIGNMENT OF POLYETHYLENE CUP INDICATED WEAR ON LINER. DOI: UNKNOWN; DOR: (B)(6) 2018; LEFT HIP.

    Patient problems: Pain

    MAUDE report 7790566 ↗

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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