TRI-LOCK GRIPTION 1012-14-100Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295001126), received between Nov 5, 2019 and Jan 19, 2021 — classified as 6 injuries.

The most frequently reported specific device problem is “Loss of Osseointegration” (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

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryJan 19, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE HIP WAS INFECTED AND HAD TO PULL EVERYTHING. DOI: UNKNOWN. DOR: (B)(6) 2021. RIGHT HIP.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 11193260 ↗
• InjuryOct 15, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT HAD INFECTION, I&D PERFORMED. IMPLANTS REMOVED AND ANTIBIOTIC SPACER PLACED. DOI: (B)(6) 2020, DOR: (B)(6) 2020, AFFECTED SIDE: LEFT HIP.

  Patient problems: No Code Available; Unspecified Infection

  MAUDE report 10684879 ↗
• InjuryJun 10, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT WAS INFECTED. DOI: (B)(6) 2019, DOR: (B)(6) 2020, RIGHT SIDE.

  Patient problems: No Code Available; Unspecified Infection

  MAUDE report 10137701 ↗
• InjuryMar 11, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PCF AND MEDICAL RECORDS RECEIVED. AFTER REVIEW OF MEDICAL RECORDS, PATIENT HAS PAIN ON THE LEFT HIP DURING PHYSICAL EXAMINATION LAST (B)(6) 2017. RECENT LABS REVEAL COBALT INCREASED FROM 20.2 TO 25. CHROMIUM IS STABLE AT 11. IT WAS 10 BEFORE. THE PATIENT HAS SIGNIFICANT FUNCTIONAL DEFICITS, RECENT VISUAL PROBLEM, TROCHANTER TENDERNESS, PAIN IN ROTATION OF THE LEG, AND LEG LENGTH DISCREPANCY. THE PATIENT AMBULATES WITH AN ANTALGIC TRENDELENBURG GAIT AND MOVES ABOUT AT A MODERATE PACE. MEDICAL RECORDS ALSO STATED A WEAR OF ARTICULAR BEARING SURFACE OF INTERNAL PROSTHETIC LEFT HIP JOINT. PATIENT WAS REVISED TO ADDRESSED LEFT FAILED TOTAL HIP ARTHROPLASTY, METAL ON METAL REACTION. OPERATIVE NOTES STATED OF METAL STAINED REACTION. THERE WAS A PARTIAL EROSION OF ABDUCTORS. NO EVIDENCE OF INFECTION. DOI: (B)(6) 2009, DOR: (B)(6) 2017, LEFT HIP.

  Patient problems: Discomfort; Foreign Body Reaction; Limited Mobility Of The Implanted Joint; No Code Available; Pain; Pocket Erosion; Visual Impairment

  MAUDE report 9818836 ↗
• InjuryNov 19, 2019Loss of Osseointegration; Osseointegration Problem; Loss of Osseointegration; Osseointegration Problem

  THE PATIENT WAS REVISED TO ADDRESS RIGHT HIP PAIN FROM FRACTURED FEMUR FROM A FALL AND LOOSENING OF THE STEM AT THE BONE TO IMPLANT INTERFACE. REPLACED TRILOCK STEM WITH LONG RECLAIM AND 8 CABLES. DOI: (B)(6) 2019. DOR: (B)(6) 2019; RIGHT HIP.

  Patient problems: Bone Fracture(s); Inadequate Osseointegration; Pain

  MAUDE report 9343482 ↗
• InjuryNov 5, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT HAD PERIPROSTHETIC FRACTURE DUE TO FALL. DOI: (B)(6) 2019; DOR: (B)(6) 2019; RIGHT HIP.

  Patient problems: Bone Fracture(s); No Code Available

  MAUDE report 9280243 ↗