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NCB® 02.03263.115Recalls & reported problems

Zimmer GmbH · NCB PP PROX FEM PLATE, L,15 H, L. 324MM · Class 2

All models of NCB (78)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
4
Deaths reported
0
Injuries reported
4
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024297524), received between Apr 16, 2020 and May 30, 2023 — classified as 4 injuries.

The most frequently reported specific device problem is “Fracture” (4 reports).

2 other recalls cover devices cleared under the same FDA submission (K100111); 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

Device problems

  • Fracture4
  • Material Integrity Problem1
  • Patient Device Interaction Problem1

Patient problems

  • Failure of Implant3
  • Bone Fracture(s)1
  • Insufficient Information1
  • No Information1

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 30, 2023Fracture; Fracture

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

    Patient problems: Failure of Implant

    MAUDE report 17017956 ↗
  • InjurySep 30, 2021Fracture; Material Integrity Problem; Fracture; Material Integrity Problem

    PATIENT WAS IMPLANTED ON RIGHT SIDE AND WAS REVISED DUE TO PLATE FRACTURE.

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

    MAUDE report 12552512 ↗
  • InjurySep 29, 2021Fracture; Patient Device Interaction Problem; Fracture; Patient Device Interaction Problem

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

    Patient problems: Failure of Implant

    MAUDE report 12546474 ↗
  • InjuryApr 16, 2020Fracture; Fracture

    NO CHANGE TO PREVIOUSLY REPORTED EVENT.

    Patient problems: No Information

    MAUDE report 9966423 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K100111. One submission often covers many models, so check the product and lot details in each record.

  • Z-0329-2020 · Oct 10, 2019 · Terminated
    Various temporary devices used during the implantation of the device system: bone fixation plates and screws, drill bits, manual surgical instruments for general use. Item Nos. 020
  • Z-0304-2020 · Oct 10, 2019 · Terminated
    NCB PERIPROSTHETIC, "NCB PP PROX FEM PLATE", Various sizes, Item Nos. 0202263009 0202263012 0202263015 0202263018 0202263021 0202263109 0202263112 0202263115 0202263118 02

Other Plate, fixation, bone devices

All Plate, fixation, bone devices →

Sources and updates

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