Kinectiv® 00-7713-012-00Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889024132658), received between Sep 10, 2020 and Mar 2, 2026 — classified as 3 injuries.

The most frequently reported specific device problem is “Implant subsidence” (1 report).

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

• InjuryMar 2, 2026Implant subsidence

  IT WAS REPORTED, DURING THE REHABILITATION PERIOD, THE STEM SUBSIDENCE OCCURRED DUE TO A SKELETAL FRACTURE. IT WAS CONFIRMED THAT NO FURTHER INFORMATION COULD BE PROVIDED.

  Patient problems: Bone Fracture(s)

  MAUDE report 24481986 ↗
• InjuryMay 13, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT PRESENTED TO PHYSICIAN APPROXIMATELY 2 WEEKS POST INITIAL RIGHT HIP PROCEDURE WITH LATERAL REDNESS IN A WELL-APPROXIMATED, ALMOST HEALED INCISION. THE PATIENT WAS PLACED ON ORAL ANTIBIOTICS AND INSTRUCTED TO RETURN IN ONE WEEK FOR A FOLLOW UP. UPON RETURN, IT WAS NOTED THAT THE INCISION WAS COMPLETELY HEALED. NO FURTHER COMPLICATIONS WERE REPORTED CONCERNING THE INCISION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Impaired Healing

  MAUDE report 11819986 ↗
• InjurySep 10, 2020Adverse 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: Adhesion(s); Bone Fracture(s); Fall; Scar Tissue; Tissue Damage

  MAUDE report 10519061 ↗

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-2365-2018 · May 30, 2018 · Terminated
  Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 10; 00-7713-010-00
• 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-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.