G7® Acetabular System 110026857Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05019279998234), received between Aug 3, 2020 and Oct 6, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 6, 2020Break; Material Integrity Problem; Break; Material Integrity Problem

  DURING THE INSPECTION OF THE KIT IN THE ZB SPAIN WAREHOUSE, IT HAS BEEN DETECTED THAT THE RING IS BROKEN. NOT PATIENT INVOLVED. NO SURGERY OCCURRED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10634756 ↗
• MalfunctionAug 3, 2020Break; Fracture; Break; Fracture

  IT WAS REPORTED THAT DURING THE INSPECTION OF THE KIT IN THE ZIMMER BIOMET SPAIN WAREHOUSE, IT HAS BEEN DETECTED THAT THE PIECE IS BROKEN. NOT PATIENT INVOLVED. NO SURGERY OCCURRED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10354664 ↗

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