Kinectiv® 00-7713-016-00Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889024132689), received between Dec 10, 2019 and Jul 1, 2024 — classified as 3 injuries.

The most frequently reported specific device problem is “Unintended Movement” (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.

• InjuryJul 1, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE. SUBSEQUENTLY, THE PATIENT WAS REVISED APPROXIMATELY 3 MONTHS LATER DUE TO PERIPROSTHETIC FRACTURE FOLLOWING A FALL. DURING THE REVISION 5 CERCLAGE WIRES WERE USED TO REDUCE AND STABILIZE THE FRACTURE. THE STEM AND HEAD WERE REPLACED WITHOUT COMPLICATIONS. IT WAS REPORTED THAT NO FURTHER INFORMATION WAS AVAILABLE.

  Patient problems: Bone Fracture(s); Failure of Implant; Hematoma

  MAUDE report 19643583 ↗
• InjuryOct 5, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY THE SURGEON THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE AND WAS REVISED APPROXIMATELY THREE MONTHS LATER DUE TO A FALL AND SUBSEQUENT PERIPROSTHETIC FEMUR FRACTURE. THERE WERE NO REPORTED SURGERY COMPLICATIONS. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Bone Fracture(s); Fall; Pain

  MAUDE report 17875535 ↗
• InjuryDec 10, 2019Unintended Movement; Unintended Movement

  IT WAS REPORTED PATIENT UNDERWENT RIGHT HIP REVISION APPROXIMATELY 4 MONTHS POST IMPLANTATION DUE TO RECURRENT DISLOCATIONS. DURING THE REVISION PROCEDURE, IT WAS NOTED THAT THE EXTERNAL ROTATORS WERE TORN FROM THEIR ATTACHMENT. ABUNDANT SCAR TISSUE, PSEUDOCAPSULE, AND IMPINGEMENT WERE ALSO NOTED. THE HEAD, NECK, AND LINER WERE REPLACED WITHOUT COMPLICATION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Host-Tissue Reaction; Scar Tissue; Tissue Damage

  MAUDE report 9443935 ↗

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.