NCB® 02.02267.010Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024484702), received between Dec 18, 2020 and Dec 18, 2020 — 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 (K113718); 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.

• InjuryDec 18, 2020Fracture; Adverse Event Without Identified Device or Use Problem; Appropriate Device Problem Term/Code Not Available; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT REVISION SURGERY DUE TO PLATE FRACTURED APPROX. 6 WEEKS AFTER IMPLANTATION.

  Patient problems: Bone Fracture(s); Failure of Implant

  MAUDE report 11036422 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K113718. One submission often covers many models, so check the product and lot details in each record.

• Z-0331-2020 · Oct 10, 2019 · Terminated
  NCB Straight Narrow Plate, various sizes, Item Nos. 0202267008 0202267010 0202267012 0202267014 0202267016 0202267018