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Kinectiv® 00-7848-012-00Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

All models of Kinectiv (21)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024137806), received between Jul 20, 2020 and Jul 20, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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

Device problems

  • Device Dislodged or Dislocated1
  • Unstable1

Patient problems

  • Joint Dislocation1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 20, 2020Unstable; Device Dislodged or Dislocated; Unstable; Device Dislodged or Dislocated

    IT WAS REPORTED PATIENT UNDERWENT A LEFT HIP REVISION APPROXIMATELY 4 YEARS POST IMPLANTATION DUE TO INSTABILITY WITH SUBSEQUENT DISLOCATIONS. DURING THE PROCEDURE A LONGER AND MORE OFFSET KINECTIV NECK AND ELEVATED LIP LINER WERE USED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

    Patient problems: Joint Dislocation

    MAUDE report 10296279 ↗

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

Other Prosthesis, hip, semi-constrained, metal/polymer, uncemented devices

All Prosthesis, hip, semi-constrained, metal/polymer, uncemented devices →

Sources and updates

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