PINNACLE GRIPTION 1217-32-066Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295010371), received between Nov 28, 2017 and Jan 15, 2026 — classified as 4 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (2 reports).

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.

• InjuryJan 15, 2026Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO INFECTED TOTAL HIP. AFFECTED SIDE: LEFT HIP.

  Patient problems: Unspecified Infection

  MAUDE report 24079198 ↗
• InjuryNov 17, 2021Use of Device Problem; Use of Device Problem

  THE PATIENT UNDERWENT PRIMARY THR SURGERY (LEFT HIP) ON TUESDAY THE (B)(6) 2021. IN REGARDS TO THE POST OPERATIVE COMPONENT POSITIONING, IT'S NOTICEABLE THAT THE PATIENT HAS NO PUBIS DUE TO A PREVIOUS SARCOMA, SO REFERENCING FOR CUP POSITIONING WAS CHALLENGING. AS A RESULT, THE PRIMARY CUP WAS NOT PLACED IN AN OPTIMAL POSITION, AND THE PATIENT HAS SUFFERED A SUBSEQUENT POST-OPERATIVE DISLOCATION. THE SURGEON ELECTED TO REVISE THE HIP (REVISION SURGERY WAS PERFORMED TODAY ¿ SATURDAY THE (B)(6) 2021). CORAIL STEM WAS UPSIZED TO A 14 HO FROM A 13 STD, AND THE PINNACLE CUP WAS REMOVED AND REVISED TO A ZIMMER/BIOMET G7 CUP.

  Patient problems: Joint Dislocation

  MAUDE report 12828457 ↗
• InjuryJun 20, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  NEW UNITY RECORD CREATED IN ORDER TO UPDATE LEGACY COMPLAINT NUMBER: (B)(4). LITIGATION PAPERS ALLEGE: ON OR ABOUT (B)(6) 2009 PATIENT UNDERWENT A LEFT TOTAL HIP ARTHROPLASTY PROCEDURE. DUE TO PATIENT'S CHRONIC PAIN AND DISCOMFORT AND OTHER SYMPTOMS, PATIENT WILL LIKELY NEED TO UNDERGO REVISION SURGERY TO REPLACE THE LEFT IMPLANT. DOI: (B)(6) 2009 - DOR: NONE REPORTED (LEFT SIDE) PATIENT IS A RESIDENT OF (B)(6). UPDATE 11/26/2012 - MEDICAL RECORDS WERE RECEIVED. PART/LOT INFORMATION WERE IDENTIFIED. PFS AND STICKER SHEETS ARE AVAILABLE ON EXTERNAL HARD DRIVE IF NEEDED FOR FURTHER REVIEW. UPDATE AD 21 MAY 2018: (B)(4) HAS BEEN RE-OPENED UNDER (B)(4) DUE TO RECEIPT OF PPF AND IMPLANT STICKER SHEET. IN ADDITION TO WHAT WERE PREVIOUSLY ALLEGED, PPF ALLEGES STROKE AND HEART ATTACK AFTER THE FIRST REVISION. DOI: (B)(6) 2009; DOR: NOT REPORTED; LEFT HIP (3RD NOT REVISED) (B)(4) - 1ST REVISION (LEFT) (B)(4) - 2ND REVISION (LEFT) (B)(4) - 1ST REVISION (RIGHT) (B)(4) - 2ND NOT REVISED (RIGHT)

  Patient problems: Cardiac Arrest; Discomfort; Infarction, Cerebral; Pain

  MAUDE report 7621313 ↗
• InjuryNov 28, 2017Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT WAS REVISED TO ADDRESS INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 7062844 ↗