Kinectiv® 00-7848-023-00Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889024137905), received between Apr 11, 2022 and Oct 5, 2023 — classified as 3 injuries.

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

• InjuryOct 5, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.

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

  MAUDE report 17875530 ↗
• InjuryOct 2, 2023Fracture; Fracture

  IT WAS REPORTED A PATIENT UNDERWENT A REVISION PROCEDURE DUE TO A DISLOCATION POST IMPLANTATION. UPON EXAMINATION OF THE EXPLANTED ITEMS, THE SURGEON NOTICED A FRACTURE IN THE NECK IMPLANT. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Failure of Implant

  MAUDE report 17852587 ↗
• InjuryApr 11, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THE PATIENT UNDERWENT INITIAL LEFT TOTAL HIP ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT WAS REVISED ONE (1) MONTH LATER DUE TO PAIN AND PERIPROSTHETIC FEMORAL FRACTURE. DURING THE REVISION, A LARGE MEDIAL FRAGMENT FROM THE LESSER TUBEROSITY TO THE MEDIAL CALCAR WAS NOTED WITH DEHISCENCE OF THE IT BAND. THE INITIAL SHELL REMAINED INTACT. ALL OTHER COMPONENTS WERE REVISED WITHOUT COMPLICATION. THREE CERCLAGE CABLES WERE PLACED FOR FRACTURE STABILIZATION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Bone Fracture(s); Muscle/Tendon Damage; Pain

  MAUDE report 14078676 ↗

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-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-2375-2018 · May 30, 2018 · Terminated
  Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 9; 00-7713-009-00
• 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.