PINNACLE GRIPTION 1217-31-062Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10603295010258), received between Aug 18, 2017 and Feb 5, 2026 — classified as 5 injuries.

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.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 5, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PINN 100 W/GRIPTION 62MM AND ALTRX NEUT 36IDX62OD WERE INVOLVED IN AN EVENT IN FINLAND WHERE REPEATED PATIENT SUBLUXATIONS WERE REPORTED, LEADING TO THE NEED FOR A CUSTOM-MADE DUAL MOBILITY LINER. THE PATIENT EXPERIENCED JOINT INSTABILITY AND SERIOUS INJURY, WITH SUBLUXATIONS AS THE CLINICAL CONSEQUENCE. THE AFFECTED SIDE WAS THE RIGHT. BOTH PRODUCTS ARE ASSOCIATED WITH HIP ACETABULAR PROCEDURES.

  Patient problems: Joint Laxity

  MAUDE report 24267587 ↗
• InjuryDec 31, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  (B)(6) FIRST REPORT OF RETRIEVALS FOR STATEMENT OF WORK FOR Q4 OF 2025. (B)(6) IS THE RESEARCH LOCATION, AND NOT THE FACILITY OF PLACEMENT. A DEPUY SYNTHES IMPLANT WAS REVISED AND REVIEWED FOR ANALYSIS. REASON FOR REVISION: "REVISION FOR INFECTION: THE ARTICULAR SURFACE OF THE FEMORAL HEAD SHOWS SEVERE METAL TRANSFER. THE NON-ARTICULAR SURFACE OF THE POLY LINER SHOWS MINOR YELLOWING. THE ARTICULAR SURFACE SHOWS MODERATE YELLOWING AND EMBEDDED METAL".

  Patient problems: Unspecified Infection

  MAUDE report 23934544 ↗
• InjuryMay 8, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  (B)(6) FIRST REPORT OF RETRIEVALS FOR STATEMENT OF WORK 10 FOR Q1 OF 2025. (B)(6) IS THE RESEARCH LOCATION, AND NOT THE FACILITY OF PLACEMENT. A DEPUY SYNTHES IMPLANT WAS REVISED AND REVIEWED FOR ANALYSIS. REASON FOR REVISION: REVISION DUE TO INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 21983976 ↗
• InjuryOct 23, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  LITIGATION ALLEGES INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 7995675 ↗
• InjuryAug 18, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  PATIENT WAS REVISED TO ADDRESS DISASSOCIATION.

  Patient problems: No Code Available

  MAUDE report 6804624 ↗