Trilogy® 65-6200-60-22Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024172579), received between Nov 19, 2019 and Nov 19, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical Problem” (1 report).

1 other recall cover devices cleared under the same FDA submission (K980711); they may or may not involve this specific model.

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.

• MalfunctionNov 19, 2019Mechanical Problem; Mechanical Problem

  IT WAS REPORTED THAT DURING AN INITIAL HIP ARTHROPLASTY, THE LINER WOULD NOT ASSEMBLE WITH THE SHELL. DIFFERENT IMPLANT WAS USED IN THE SURGERY. ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9342232 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K980711. One submission often covers many models, so check the product and lot details in each record.

• Z-0770-2013 · Sep 14, 2012 · Terminated
  Trilogy F/M Acetabular Shell without holes SOLID HA. Several ODs: 38MM, 40MM, 42MM, 44MM, 46MM, 48MM, 50MM, 52MM, 54MM, 56MM, 58MM, 60MM, 62MM, 64MM, 66MM, 68MM, 70MM. The Trilogy