Kinectiv® 00-7713-009-00Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024132627), received between Oct 15, 2021 and Oct 24, 2025 — classified as 4 injuries.

The most frequently reported specific device problem is “Material Erosion” (2 reports).

4 other recalls cover devices cleared under the same FDA submission (K063251, K182678); they may or may not involve this specific model.

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 18, 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.

• InjuryOct 24, 2025Material Erosion; Naturally Worn; Material Erosion; Naturally Worn

  NO ADDITIONAL INFORMATION AVAILABLE FOR THE REPORTED EVENT.

  Patient problems: Joint Dislocation; Metal Related Pathology

  MAUDE report 23377926 ↗
• InjuryMar 10, 2025Degraded; Adverse Event Without Identified Device or Use Problem; Degraded; Adverse Event Without Identified Device or Use Problem

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

  Patient problems: Unspecified Infection

  MAUDE report 21558447 ↗
• InjuryMar 14, 2022Material Erosion; Naturally Worn; Material Erosion; Naturally Worn

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION PROCEDURE APPROXIMATELY THREE (3) YEARS AND FOUR (4) MONTHS POST IMPLANTATION DUE TO WEAR. NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Failure of Implant; Metal Related Pathology

  MAUDE report 13758353 ↗
• InjuryOct 15, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

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

  Patient problems: Bone Fracture(s)

  MAUDE report 12638898 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K063251, K182678. One submission often covers many models, so check the product and lot details in each record.

• Z-2375-2018 · May 30, 2018 · Terminated
  Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 9; 00-7713-009-00
• Z-2364-2018 · May 30, 2018 · Terminated
  Zimmer M/L Taper Hip Prosthesis With Kinectiv Technology Cementless, Size 6; 00-7713-006-00
• Z-2365-2018 · May 30, 2018 · Terminated
  Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 10; 00-7713-010-00
• Z-1617-2009 · May 29, 2009 · Terminated
  Zimmer Kinectivo Technology Modular Neck, BB, 12/14 neck taper, sterile, Zimmer, Warsaw, IN; Catalog Number: 00-7848-022-01. Orthopedic implant used in total hip arthroplasty.