Cable-Ready® 2232-05-18Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024039537), received between Nov 5, 2024 and Jul 11, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (1 report).

1 other recall cover devices cleared under the same FDA submission (K151907); 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJul 11, 2025Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A PRIMARY SURGERY APPROXIMATELY ONE (1) YEAR AND THREE (3) MONTHS AGO TO RECEIVE A HIP ARTHROPLASTY AND A CABLE READY GTR PLATE AND CABLES. WHEN THE CASE WAS DONE, THERE WAS A NON-ZB BONE GRAFT PUT IN BETWEEN THE CABLE READY PLATE AND THE HIP STEM. SUBSEQUENTLY, THE GRAFT DID NOT TAKE WHICH CAUSED THE PLATE AND CABLES TO BECOME LOOSE. THE PATIENT UNDERWENT A REOPERATION APPROXIMATELY THREE (3) WEEKS AGO TO REMOVE THE PLATE AND CABLES. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Aseptic loosening

  MAUDE report 22480275 ↗
• InjuryNov 5, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THE PATIENT UNDERWENT AN INITIAL RIGHT TOTAL HIP ARTHROPLASTY ON AN UNKNOWN DATE WITH UNKNOWN IMPLANTS. SUBSEQUENTLY, THE PATIENT SUSTAINED A PERIPROSTHETIC FRACTURE RESULTING IN AN ORIF OF THE RIGHT PROXIMAL FEMUR WITH PLATE, WIRES, AND SCREWS IMPLANTED. SUBSEQUENTLY, THE PATIENT WAS REVISED DUE TO A GREATER TROCHANTERIC FRACTURE. NO FURTHER DETAILS PROVIDED.

  Patient problems: Bone Fracture(s)

  MAUDE report 20614153 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K151907. One submission often covers many models, so check the product and lot details in each record.

• Z-0327-2020 · Oct 10, 2019 · Terminated
  CABLE-READY SHORT GTR and CABLE-READY LONG GTR, Item Nos. 00223200201 00223200202