NCB® 02.02263.015Recalls & reported problems
Zimmer GmbH · NCB PP PROX FEM PLATE, R,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
- 8
- Deaths reported
- 0
- Injuries reported
- 8
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00889024292703), received between Dec 11, 2019 and Apr 24, 2026 — classified as 8 injuries.
The most frequently reported specific device problem is “Fracture” (8 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.
Reports received per month
Most reported problems
Device problems
- Fracture8
- Material Integrity Problem1
Patient problems
- Failure of Implant5
- Bone Fracture(s)2
- Pain2
- No Code Available1
- Periprosthetic fracture1
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
InjuryApr 24, 2026Fracture
No further event information available at the time of this report.
Patient problems: Periprosthetic fracture
MAUDE report 24979502 ↗InjuryApr 21, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Failure of Implant
MAUDE report 21874627 ↗InjuryJun 21, 2024Fracture; Fracture
IT WAS REPORTED THAT THE PATIENT EXPERIENCED A REVISION SURGERY DUE TO BROKEN OF NCB PLATE APPROXIMATELY TWO-AND-A-HALF-MONTHS POST IMPLANTATION. DILIGENCE IS COMPLETED AND NO FURTHER INFORMATION ON THE REPORTED EVENT HAS BEEN PROVIDED.
Patient problems: Failure of Implant
MAUDE report 19584157 ↗InjuryMar 23, 2022Fracture; Material Integrity Problem; Fracture; Material Integrity Problem
IT WAS REPORTED THAT THERE WAS A REVISION DUE TO IMPLANT FRACTURE AND PAIN.
Patient problems: Failure of Implant; Pain
MAUDE report 13858494 ↗InjuryOct 12, 2020Fracture; Fracture
INVESTIGATION RESULTS ARE NOW AVAILABLE.
Patient problems: Bone Fracture(s); Failure of Implant
MAUDE report 10661500 ↗InjuryOct 9, 2020Fracture; Fracture
INVESTIGATION RESULTS ARE NOW AVAILABLE.
Patient problems: Bone Fracture(s); Failure of Implant
MAUDE report 10655689 ↗InjuryAug 12, 2020Fracture; Fracture
PATIENT WAS IMPLANTED ON THE RIGHT SIDE AND UNDERWENT REVISION SURGERY DUE TO IMPLANT FRACTURE.
Patient problems: No Code Available
MAUDE report 10395520 ↗InjuryDec 11, 2019Fracture; Fracture
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 · TerminatedVarious 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 · TerminatedNCB 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
- Lapiplasty System 2 SK14Treace Medical Concepts, Inc. · Plate, Fixation, Bone260 reports
- PRECICE® Plating System LP4.5-PRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls6 reports
- PRECICE® Plating System LP4.5-MLT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls5 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page