G7® Dual Mobility 110024732Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00880304712881), received between Feb 17, 2026 and Feb 17, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 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.

• MalfunctionFeb 17, 2026Detachment of Device or Device Component

  IT WAS REPORTED THAT, AT THE START OF SURGERY, SCRIBED NURSE REARRANGED PROVISIONAL LINERS IN G7 DM TRAY BECAUSE THEY WERE MIXED UP, AND THE SCREWS OF THE LINER E AND LINER F FELL OUT ON TABLE. SURGERY WAS NOT DELAYED SINCE WE DID NOT USE THESE SIZES. NO SCREWS FELL INTO PATIENT BECAUSE IT WAS REALIZED BEFORE OPENING. INVESTIGATION OF THE REPORTED DEVICES LATER FOUND WEAR DAMAGE PRESENT ON BOTH DEVICES. DILIGENCE IS COMPLETED AND ALL AVAILABLE INFORMATION HAS BEEN PROVIDED AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24366918 ↗

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