PINNACLE GRIPTION 1217-30-068Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295010067), received between Sep 17, 2018 and Dec 5, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Osseointegration Problem” (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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryDec 5, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  INFECTION IN HIP JOINT REPLACEMENT, PREVIOUS WASHOUTS ATTEMPTED WITH INFECTION NOT RESOLVED. DECISION WAS MADE TO REMOVE ALL IMPLANTS AND REPLACE WITH CEMENT LOADED WITH ANTIBIOTICS TO DEAL WITH THE INFECTION. PLASTIC SURGEON INVOLVED TO MANAGE TISSUE LOSS. PLAN IS TO BRING HIM BACK TO THEATRE ONCE THE INFECTION IS RESOLVED AND THE WOUND HAS HEALED. IMPLANTS IN PLACE ARE RECLAIM WITH PINNACLE MULTIHOLE CUP AND BIMENTUM SHELL CEMENTED IN PLACE.

  Patient problems: Unspecified Infection

  MAUDE report 18267872 ↗
• InjurySep 17, 2018Osseointegration Problem; Osseointegration Problem

  PPF ALLEGE LOOSENING OF CUP AND DISLOCATION. IT WAS ALSO INDICATED IN THE REVISION IMPLANTS THAT WAS REVISED. DOI: (B)(6) 2008; DOR: (B)(6) 2008; (RIGHT HIP).

  Patient problems: Inadequate Osseointegration

  MAUDE report 7880786 ↗