G7 Acetabular Liner 010000811Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00880304526020), received between Dec 1, 2020 and Nov 25, 2024 — classified as 1 injury, 3 malfunctions.

The most frequently reported specific device problem is “Difficult to Insert” (3 reports).

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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 25, 2024Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING A HIP PROCEDURE, THE LINER WOULD NOT FIT THE CUP WHILE IMPACTING. THERE WAS A 33 MINUTE DELAY. ANOTHER LINER WAS OPENED AND FIT INTO THE CUP CORRECTLY THERE WAS NO KNOWN IMPACT OR CONSEQUENCES TO THE PATIENT. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20772305 ↗
• MalfunctionApr 3, 2024Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING AN INITIAL HIP ARTHROPLASTY THAT THE INSERT WAS IMPACTED SEVERAL TIMES WHILE TRYING TO INSERT AND AFTER APPROXIMATELY FORTY (40) MINUTES THE LINER WAS UNABLE TO BE INSERTED. THE PATIENT BEGAN TO BLEED, AND THE SURGEON DECIDED TO OPEN ANOTHER INSERT AND ANOTHER FEMORAL HEAD IN THE NEXT DIAMETER, BEING THE OPTION THAT WAS AVAILABLE AT THE TIME. THE CUP WAS SUCCESSFULLY IMPLANTED WITHOUT ANY PROBLEMS. SURGICAL TECHNIQUE OF THE PRODUCTS WAS UTILIZED.

  Patient problems: Hemorrhage/Blood Loss/Bleeding

  MAUDE report 19032667 ↗
• MalfunctionApr 12, 2022Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING AN INITIAL HIP ARTHROPLASTY, THE LINER WOULD NOT SEAT INTO THE CUP. AN ADDITIONAL LINER WAS USED TO COMPLETE THE PROCEDURE WITHOUT FURTHER ISSUES. NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14084665 ↗
• InjuryDec 1, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Joint Dislocation

  MAUDE report 10928588 ↗