G7® Acetabular System 110017106Recalls & reported problems
Biomet Orthopedics, LLC · Class 2 · Implant
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00880304672130), received between Feb 8, 2022 and Jan 5, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device Contaminated During Manufacture or Shipping” (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
- Device Contaminated During Manufacture or Shipping1
- Difficult to Insert1
- Separation Failure1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 5, 2026Device Contaminated During Manufacture or Shipping
IT WAS REPORTED THAT WHITE DUST WAS FOUND ON THE STERILE PACKAGING BEFORE ENTERING THE STERILE FIELD. THE CUP WAS NOT USED DUE TO THE SURGEON CONCERNS FOR STERILITY. THERE WAS NO PATIENT INVOLVEMENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23960601 ↗MalfunctionApr 17, 2024Separation Failure; Separation Failure
IT WAS REPORTED THAT THE SCREW HOLE CAPS COULD NOT BE REMOVED FROM THE SHELL. THE EVENT HAPPENED DURING AN INITIAL SURGERY. SURGICAL TECHNIQUE WAS UTILIZED. THERE WAS NO PATIENT IMPACT. THERE WAS NO MEDICAL OR SURGICAL INTERVENTION. THERE WAS NO SURGICAL DELAY AND NO SURGICAL COMPLICATIONS. FOREIGN BODY WAS NOT RETAINED. NO ADDITIONAL INFORMATION AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19124102 ↗MalfunctionFeb 8, 2022Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT DURING SURGERY, THE LINER IMPLANT COULD NOT BE ASSEMBLED WITH THE CUP IMPLANT. THE CUP AND LINER WERE REMOVED AND REPLACED. NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13480687 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.