Cable-Ready® 2232-01-18Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00889024039315), received between Dec 1, 2025 and Jun 8, 2026 — classified as 4 injuries, 1 malfunction.

The most frequently reported specific device problem is “Fracture” (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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 8, 2026Fracture

  IT WAS REPORTED THAT DURING A PROCEDURE, THE CABLE BROKE WHEN APPLYING TENSION TO THE SCREW. SURGEON NOTES THEY WERE TIGHTENING THE CABLE AS PER THEIR USUAL PRACTICE AND TORQUE, AND THE CABLE BROKE. THERE WAS NO DEVIATION FROM THE SURGICAL TECHNIQUE. A NEW CABLE WAS OPENED AND USED WITHOUT ISSUE. NO PATIENT CONSEQUENCES WERE REPORTED AS A RESULT OF THE EVENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25428151 ↗
• InjuryDec 1, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Nonunion/Delayed-union Bone Fracture; Pain

  MAUDE report 23680219 ↗
• InjuryDec 1, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Nonunion/Delayed-union Bone Fracture; Pain

  MAUDE report 23680191 ↗
• InjuryDec 1, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Nonunion/Delayed-union Bone Fracture; Pain

  MAUDE report 23680189 ↗
• InjuryDec 1, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Nonunion/Delayed-union Bone Fracture; Pain

  MAUDE report 23680179 ↗

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