PINNACLE GRIPTION 1217-17-056Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10603295009467), received between Sep 26, 2018 and Sep 4, 2024 — classified as 7 injuries.

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 18, 2026.

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• InjurySep 4, 2024Use of Device Problem; Use of Device Problem

  ADDITIONAL INFORMATION WAS RECEIVED: NO SURGICAL DELAY.

  Patient problems: Insufficient Information

  MAUDE report 20136012 ↗
• InjuryApr 1, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT EXPERIENCED PAIN, SEVERE SEPSIS, SEPTICEMIA, INFECTION. GENERALIZED WEAKNESS, HYPOXIA, APNEA, ASTHMA, AND PNEUMONIA. DOI: (B)(6) 2016. DOR: NONE REPORTED, (RIGHT HIP).

  Patient problems: Apnea; No Code Available; Pain; Pneumonia; Sepsis; Unspecified Infection; Weakness

  MAUDE report 9909105 ↗
• InjuryFeb 10, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED TO ADDRESS PAIN. DOI: (B)(6) 2018; DOR: (B)(6) 2020; RIGHT HIP.

  Patient problems: No Code Available; Pain

  MAUDE report 9688662 ↗
• InjuryApr 24, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  CLAIM AND MEDICAL RECORDS RECEIVED. AFTER REVIEW OF CLAIM AND MEDICAL RECORDS, IT WAS STATED THAT THE PATIENT WAS REVISED TO ADDRESS INFECTION WITH BONE ALLOGRAFTING. OPERATIVE NOTE REPORTED A LARGE ABSCESS IN THE SUBCUTANEOUS TISSUE, DEAD TISSUES AND PUS IN THE ACETABULAR COMPONENT. DEAD BONE WERE REMOVED FROM THE FEMUR; HOWEVER, STEM WAS INTACT THUS LEFT IN SITU. ANTIBIOTIC SPACER WAS IMPLANTED INTO THE AFFECTED SIDE. DOI: (B)(6) 2008; DOR: (B)(6) 2009; LEFT HIP.

  Patient problems: Abscess; Injury; Necrosis; No Code Available; Tissue Damage; Unspecified Infection

  MAUDE report 8543995 ↗
• InjuryFeb 12, 2019Malposition of Device; Malposition of Device

  THE PATIENT WAS REVISED TO ADDRESS DISLOCATION.

  Patient problems: No Code Available

  MAUDE report 8330861 ↗
• InjuryJan 8, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PPF ALLEGES INFECTION AND LOOSENING OF STEM.

  Patient problems: No Code Available; Unspecified Infection

  MAUDE report 8228206 ↗
• InjurySep 26, 2018Separation Problem; Separation Problem

  THE PATIENT WAS REVISED TO ADDRESS UNSTABLE HIP. IT WAS ALSO REPORTED THAT THE LINER DISASSOCIATED FROM THE CUP. DOI: (B)(6) 2017; DOR: (B)(6) 2018; LEFT HIP.

  Patient problems: Joint Disorder; Not Applicable

  MAUDE report 7912329 ↗