NCB® 02.02264.115Recalls & reported problems
Zimmer GmbH · NCB PP DIST FEM PLATE, L,15 H, L. 317MM · Class 2
All models of NCB (78)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00889024292901), received between Jun 3, 2019 and Aug 17, 2021 — classified as 5 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 16, 2026.
Most reported problems
Device problems
- Fracture4
- Insufficient Device Problem Information1
- Material Integrity Problem1
Patient problems
- Failure of Implant2
- Fall1
- No Information1
- Nonunion/Delayed-union Bone Fracture1
- Unspecified Infection1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryAug 17, 2021Fracture; Material Integrity Problem; Fracture; Material Integrity Problem
INVESTIGATION RESULTS ARE NOW AVAILABLE.
Patient problems: Fall; Nonunion/Delayed-union Bone Fracture
MAUDE report 12330273 ↗InjuryMar 17, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
InjuryMar 17, 2020Fracture; Fracture
InjuryOct 4, 2019Fracture; Fracture
InjuryJun 3, 2019Fracture; Fracture
IT WAS REPORTED THAT PATIENT UNDERWENT REVISION SURGERY DUE TO IMPLANT FRACTURE.
Patient problems: Failure of Implant
MAUDE report 8662404 ↗
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-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 0202263121
- 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
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-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive 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-PLF40Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-PRT42Nuvasive 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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