G7® Longevity® 20103604Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889024518735), received between Mar 5, 2024 and Aug 10, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Difficult or Delayed Separation” (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.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 10, 2026Difficult to Insert; Difficult or Delayed Separation

  It was reported that during an initial hip procedure, the liner could not be implanted properly after multiple attempts. When implanted, the liner was not aligned with the edge of the cup and it appeared crooked. Repeated attempts to implant the liner failed to resolve the issue, resulting in loosening of the acetabular cup. It was decided to remove the liner. An attempt to remove the liner with instruments was unsuccessful. A threaded wrench was used to remove the liner. Two screws were implanted to stabilize the cup and a new liner was successfully implanted. There was a 20 minute delay.There was no known impact or consequences to the patient.Attempts have been made and no further information has been provided.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50191961 ↗
• MalfunctionJul 9, 2024Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem

  IT WAS REPORTED THAT WHEN OPENING THE PACKAGING, A HAIR WAS FOUND INSIDE THE STERILE PACKAGING. THERE WAS NO HARM OR HEALTH IMPACT TO THE PATIENT. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19700397 ↗
• MalfunctionMar 5, 2024Packaging Problem; Packaging Problem

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18838224 ↗