G7® Acetabular System 110026854Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05019279999408), received between Sep 1, 2021 and Sep 1, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Activation, Positioning or Separation Problem” (1 report).

1 other recall cover devices cleared under the same FDA submission (K150522); 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 16, 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.

• MalfunctionSep 1, 2021Activation, Positioning or Separation Problem; Activation, Positioning or Separation Problem

  IT WAS REPORTED THAT THE BEARING INSERTER RING BECAME LODGED BETWEEN LINER AND CUP RESULTING IN DEFORMATION OF THE RING. ANOTHER INSTRUMENT WAS READILY AVAILABLE AND OPENED TO SOLVE THE PROBLEM RESULTING IN A MINIMAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12405790 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K150522. One submission often covers many models, so check the product and lot details in each record.

• Z-1284-2023 · Feb 6, 2023 · Open, Classified
  G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462