NCB® 02.02263.201Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024292796), received between Jun 18, 2020 and Oct 1, 2020 — classified as 2 injuries.

The most frequently reported specific device problem is “Fracture” (2 reports).

2 other recalls cover devices cleared under the same FDA submission (K120772); 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.

• InjuryOct 1, 2020Fracture; Fracture

  PATIENT WAS IMPLANTED ON THE RIGHT SIDE AND UNDERWENT REVISION SURGERY DUE TO IMPLANT FRACTURE.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 10612124 ↗
• InjuryJun 18, 2020Fracture; Fracture

  PATIENT WAS IMPLANTED ON THE RIGHT SIDE AND EXPERIENCED IMPLANT FRACTURE. THE PATIENT HAS BEEN SCHEDULED FOR A REVISION SURGERY.

  Patient problems: No Code Available

  MAUDE report 10167380 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K120772. One submission often covers many models, so check the product and lot details in each record.

• Z-0338-2020 · Oct 10, 2019 · Terminated
  cable button for NCB Polyaxial Locking Plate, 2.5 mm Hex Drive, Item No. 47223206001
• Z-0330-2020 · Oct 10, 2019 · Terminated
  Connection Screw for NCB Plate, Item No. 0202266002