G7® Acetabular System 110017102Recalls & reported problems
Biomet Orthopedics, LLC · Class 2 · Implant
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00880304672093), received between Nov 17, 2020 and Jan 28, 2026 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Difficult to Insert” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
- Difficult to Insert1
Patient problems
- Ambulation or Postural Difficulties1
- No Known Impact Or Consequence To Patient1
- Pain1
- Pulmonary Embolism1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJan 28, 2026Adverse Event Without Identified Device or Use Problem
NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.
Patient problems: Ambulation or Postural Difficulties; Pain
MAUDE report 24198956 ↗InjuryJan 10, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL LEFT TOTAL HIP ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT DEVELOPED AN ACUTE PULMONARY EMBOLISM 4 DAYS LATER. THE PATIENT WAS ADMITTED TO THE HOSPITAL AND TREATED WITH MEDICATION. PATIENT WAS SENT HOME IN STABLE CONDITION WITH HOME HEALTH CARE AND IS INSTRUCTED TO STAY ON MEDICATION FOR 3 MONTHS. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Pulmonary Embolism
MAUDE report 18485220 ↗MalfunctionNov 17, 2020Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT DURING A HIP PROCEDURE, THE TRILOGY SCREW WENT ALL THE WAY THROUGH THE SCREW HOLE ON THE G7 SHELL. THERE WAS NO REPORTED HARM OR INJURY TO THE PATIENT AND THE DEVICE REMAINS IMPLANTED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10850794 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.