PINNACLE GRIPTION 1217-17-054Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295009450), received between Dec 19, 2018 and Dec 19, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Material Disintegration” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryDec 19, 2018Material Disintegration; Noise, Audible; Separation Problem; Material Disintegration; Noise, Audible; Separation Problem

  IT WAS REPORTED THAT THE PATIENT PRESENTED TO THE SURGEON WITH PAIN AND CLICKING IN HER HIP. ON X-RAY, IT APPEARED THAT THE POLY HAD WORN THRU. KNOWING IT HAD ONLY BEEN IN 1.5 YEARS, THIS WAS LIKELY NOT THE CASE. THE PATIENT HAD NO RECOLLECTION OF A TRAUMATIC EVENT, NEVERTHELESS THE SURGEON SUSPECTED THAT THE LINER SPUN OUT AT ONE POINT. UPON EXAMINATION IN THE OR, THE METAL HEAD HAD INDEED BEEN ARTICULATING ON THE METAL SHELL AND WORN DOWN THE METAL ON THE RIM OF THE SHELL. THE CUP WAS REMOVED BECAUSE THE LOCKING TAPER IN THE SHELL HAD BEEN COMPROMISED. THE 54 DEEP PROFILE CUP WAS REPLACED WITH A 56 MULTI-GRIP WITH A 40 LINER AND METAL +5 HEAD.

  Patient problems: No Code Available; Pain

  MAUDE report 8181944 ↗