9 Hole VL Gridlock Fibula Plate 300-60-002Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00812926025445), received between Apr 28, 2017 and Apr 28, 2017 — classified as 1 malfunction.

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

1 other recall cover devices cleared under the same FDA submission (K160177); 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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 28, 2017Break

  THE ANKLE FRACTURE PLATE WAS IMPLANTED WITHIN THE LAST 4 MONTHS, ACCORDING TO THE SALES REPRESENTATIVE. THE PATIENT FELL 3 TIMES WITH THE PLATE AND CAME BACK TO THE ER AFTER THE LAST FALL, WHICH LED TO AN X-RAY THAT SHOWED THE BROKEN PLATE. THE DOCTOR REMOVED AND REPLACED THE PLATE.

  Patient problems: Fall

  MAUDE report 6529655 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K160177. One submission often covers many models, so check the product and lot details in each record.

• Z-1613-2020 · Jul 19, 2018 · Terminated
  Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Gridlock Ankle Plating System, Model 320-01-100. The firm name on the label is Tri