PINNACLE GRIPTION 1217-17-062Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295009498), received between Aug 11, 2017 and Jun 20, 2019 — classified as 2 injuries.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (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.

• InjuryJun 20, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AFTER REVIEW OF MEDICAL RECORDS, THE PATIENT WAS REVISED TO ADDRESS RECURRENT SUPERFICIAL HEMATOMA. THE PATIENT HAD PREVIOUSLY UNDERGONE 5 TO 6 ASPIRATIONS TO TREAT THE HEMATOMA. OPERATIVE FINDINGS INCLUDE A LARGE HEMATOMA AND A RENT IN THE DEEP TISSUE ANTERIOR TO THE TROCHANTER AND EXTENDING INTO THE DEEP AREA OF THE HIP. DOI: (B)(6) 2010 - DOR: NO REVISION - DOE: (B)(6) 2011 (LEFT HIP).

  Patient problems: Hematoma; No Code Available

  MAUDE report 8716733 ↗
• InjuryAug 11, 2017Loss of or Failure to Bond; Loss of or Failure to Bond

  PATIENT WAS REVISED TO ADDRESS PAIN AND LOOSENING OF THE CUP COMPONENT AT BONE TO IMPLANT INTERFACE.

  Patient problems: Inadequate Osseointegration; No Code Available; Pain

  MAUDE report 6788521 ↗