PINNACLE 1219-36-066Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295014515), received between Jul 10, 2024 and Sep 6, 2024 — classified as 2 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.

• InjurySep 6, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED WITH HEAD AND LINER DUE TO INSTABILITY. DOI: UNKNOWN. DOR: (B)(6) 2024. AFFECTED SIDE: LEFT HIP.

  Patient problems: Joint Laxity

  MAUDE report 20158782 ↗
• InjuryJul 10, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THIS IS A LIMITED REVIEW OF MEDICAL RECORDS THAT PERTAINS TO A NON MOM CONSTRUCT AFTER 1ST REVISION WAS DONE. ON (B)(6) 2015, THE PATIENT HAD A REVISION RIGHT HIP STICKER PAGE 13 OF 20 A DEPUY PINNACLE MARATHON POLY LINER WAS INSERTED ALONG WITH COMPETITOR STEM/FEMORAL HEAD. (B)(4). ON (B)(6) 2015 THE PATIENT HAD A CLOSED REDUCTION OF RIGHT TOTAL HIP TO ADDRESS DISLOCATED RIGHT HIP. (ADD TO NEXT PC). ON (B)(6) 2015 THE PATIENT HAD A REVISION RIGHT HIP ARTHROPLASTY TO ADDRESS RECURRENT INSTABILITY. THE HEAD AND LINER WERE REVISED, AND CONVERTED TO A ¿CAPTURED¿ LINER (LOCKING). PATIENT RETAINED THEIR DEPUY CUP AND COMPETITOR STEM. DOI: (B)(6) 2015. DOR: (B)(6) 2015. RIGHT HIP SECOND REVISION.

  Patient problems: Joint Dislocation; Joint Laxity

  MAUDE report 19711288 ↗