PINNACLE GRIPTION 1217-31-060Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295010241), received between Aug 10, 2017 and Apr 24, 2026 — classified as 4 injuries.

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 18, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryApr 24, 2026Use of Device Problem

  IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO INSTABILITY. CUP APPEARS TO BE VERTICAL AND OVERLY ANTEVERTED. PATIENT ALSO HAS SPINAL/PELVIC ISSUES. DOI: (B)(6) 2026. DOR: (B)(6) 2026. AFFECTED SIDE: LEFT HIP.

  Patient problems: Joint Laxity

  MAUDE report 24983887 ↗
• InjuryFeb 16, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED TO ADDRESS UNSTABLE AND DISLOCATED. DOI: UNKNOWN, DOR: (B)(6) 2021, AFFECTED SIDE: UNKNOWN.

  Patient problems: Joint Laxity

  MAUDE report 11331686 ↗
• InjuryDec 14, 2018Loss of Osseointegration; Osseointegration Problem; Loss of Osseointegration; Osseointegration Problem

  PFS ALLEGES PAIN AND DIFFICULTY TO WALK. AFTER REVIEW OF MEDICAL RECORDS, THERE WERE NO NEW ALLEGATION REPORTED. ADDED PATIENT HEIGHT AND WEIGHT.

  Patient problems: Discomfort; Inadequate Osseointegration; No Code Available; Pain; Tissue Damage

  MAUDE report 8165526 ↗
• InjuryAug 10, 2017Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT WAS REVISED TO ADDRESS PAIN.

  Patient problems: Pain

  MAUDE report 6784337 ↗