G7® Vivacit-E® 30123207Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00889024520455), received between Sep 19, 2024 and Jul 18, 2025 — classified as 3 injuries, 3 malfunctions.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 18, 2025Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT TWO LINERS COULD NOT BE IMPLANTED INTO THE CUP DURING THE PROCEDURE. ANOTHER TYPE OF LINER WAS USED TO COMPLETE THE PROCEDURE. SURGERY WAS DELAYED ABOUT 120 MINUTES. 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 22541737 ↗
• MalfunctionJul 18, 2025Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT TWO LINERS COULD NOT BE IMPLANTED INTO THE CUP DURING THE PROCEDURE. ANOTHER TYPE OF LINER WAS USED TO COMPLETE THE PROCEDURE. SURGERY WAS DELAYED ABOUT 120 MINUTES. 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 22541604 ↗
• InjuryMar 25, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT APPROXIMATELY ONE DAY POST-IMPLANTATION, THE PATIENT UNDERWENT A LEFT HIP OPEN REPOSITIONING DUE TO DISLOCATION FOLLOWING A SYNCOPE EVENT AND FALL. THE TORN JOINT CAPSULE WAS REPAIRED AND JOINT REPOSITIONED WITHOUT COMPLICATIONS. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Joint Dislocation

  MAUDE report 21688794 ↗
• InjuryNov 27, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION PROCEDURE 19 DAYS POST IMPLANTATION DUE TO AN INFECTION AND SUBLUXATION OF THE HEAD AND LINER. PATIENT WAS NOTED TO HAVE A POSITIVE CULTURE FOR ENTEROCOCCUS FAECALIS PROTEUS MIRABILIS. PATIENT WAS GIVEN DICLOXACILLIN BY MOUTH FOR APPROXIMATELY 3 MONTHS. IT WAS NOTED DURING THE REVISION PROCEDURE, THE SURGEON NOTED NECROTIC INFECTED TISSUE. THERE IS NO ADDITIONAL INFORMATION AT THE TIME OF THIS REPORT.

  Patient problems: Bacterial Infection; Subluxation; Tissue Breakdown

  MAUDE report 20798353 ↗
• MalfunctionNov 1, 2024Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT THE G7 HIGHWALL LINER DID NOT FIT INTO THE CUP. THE SURGERY WAS COMPLETED WITH ANOTHER LINER. NO KNOWN IMPACT OR CONSEQUENCE TO THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20586465 ↗
• InjurySep 19, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: Blister; Fever; Joint Dislocation; Pain; Tissue Breakdown; Unspecified Infection

  MAUDE report 20256879 ↗