Kinectiv® 00-7848-030-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024509535), received between Feb 14, 2023 and Feb 14, 2023 — classified as 1 injury.

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

1 other recall cover devices cleared under the same FDA submission (K071856, 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 16, 2026.

Most reported problems

Recent adverse event reports

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

• InjuryFeb 14, 2023Fracture; Fracture

  IT WAS REPORTED A REVISION SURGERY WAS PERFORMED DUE TO A BROKEN MODULAR NECK IMPLANT. AN ML TAPER STEM WITH KINECTIV WAS USED IN THE INITIAL SURGERY THAT WAS SUBSEQUENTLY REVISED AND REPLACED APPROXIMATELY TWO AND A HALF YEARS YEARS LATER DUE TO MODULAR NECK FRACTURE. THE PHOTOS OF THE REMOVED IMPLANTS SUGGESTED THAT THE EDGES OF THE CUPS HAD CONTACTED TO THE NECK IMPLANT AND THEN FRACTURED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Failure of Implant

  MAUDE report 16371511 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K071856, K182678. One submission often covers many models, so check the product and lot details in each record.

• Z-1699-2015 · May 18, 2015 · Terminated
  M/L Taper with Kinectiv Technology. prosthesis, hip, semi-constrained (metal uncemented acetabular component) Product Usage: Usage: Total hip replacement for the following: sever