NCB® 02.03260.105Recalls & reported problems
Zimmer GmbH · NCB PLATE FOR FEMUR, LEFT, 5 HOLES · Class 2
All models of NCB (78)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024297395), received between Feb 19, 2021 and Feb 19, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (1 report).
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
- Fracture1
- Migration1
- Migration or Expulsion of Device1
- Naturally Worn1
Patient problems
- Bone Fracture(s)1
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 19, 2021Fracture; Migration or Expulsion of Device; Naturally Worn; Migration; Fracture; Migration or Expulsion of Device; Naturally Worn; Migration
PATIENT WAS IMPLANTED ON THE RIGHT SIDE AND UNDERWENT A REVISION SURGERY DUE TO PERIPROSTHETIC FRACTURE, IMPLANT FRACTURE AND WEAR BETWEEN THE TWO DISTAL SCREWS AND THE NCB PLATE LEADING TO THE MIGRATION OF THE NCB PLATE. IT WAS ALSO NOTED THAT HIP GAVE AWAY AFTER LIGHT EXERCISE ON FEB 01, 2021 WITHOUT ANY TRAUMA OR FALL.
Patient problems: Bone Fracture(s); Failure of Implant
MAUDE report 11347200 ↗
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- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-MLT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-MRT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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