NCB® 02.02263.115Recalls & 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
- 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 00889024292765), received between Dec 19, 2019 and Apr 3, 2025 — 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
Patient problems
- Failure of Implant6
- No Code Available2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Bone Fracture(s)1
- Insufficient Information1
- Osteopenia/ Osteoporosis1
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
InjuryApr 3, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Failure of Implant
MAUDE report 21762826 ↗InjuryOct 30, 2024Fracture; Fracture
IT WAS REPORTED PATIENT UNDERWENT REVISION APPROXIMATELY 1 MONTH POST IMPLANTATION DUE TO THE NCB PP PLATE BREAKING OFF IN THE BODY. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: Failure of Implant
MAUDE report 20566767 ↗InjuryJan 10, 2024Fracture; Fracture
IT WAS REPORTED THAT THE PATIENT HAD A REVISION SURGERY DUE TO BROKEN IMPLANT, APPROXIMATELY FOUR (4) MONTHS AFTER IMPLANTATION. DUE DILIGENCE HAS BEEN COMPLETED FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION HAS BEEN RECEIVED.
Patient problems: Failure of Implant
MAUDE report 18486689 ↗InjuryDec 11, 2023Fracture; Fracture
NO ADDITIONAL EVENT INFORMATION.
Patient problems: Failure of Implant; Insufficient Information
MAUDE report 18301034 ↗InjuryAug 8, 2023Fracture; Fracture
NO ADDITIONAL EVENT INFORMATION.
Patient problems: Failure of Implant; Osteopenia/ Osteoporosis
MAUDE report 17478351 ↗InjuryDec 29, 2020Fracture; Fracture
PATIENT WAS IMPLANTED ON THE LEFT SIDE AND PLANNED FOR REVISION SURGERY DUE TO IMPLANT FRACTURE. THE BONE QUALITY WAS VERY POOR, BECAUSE OF THE PSEUDARTHROSIS AND THEREFORE THE PLATE WAS BROKEN.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Failure of Implant
MAUDE report 11088109 ↗InjuryOct 12, 2020Fracture; Fracture
InjuryDec 19, 2019Fracture; Fracture
PATIENT WAS IMPLANTED ON THE LEFT SIDE AND UNDERWENT REVISION SURGERY DUE TO PERIPROSTHETIC FRACTURE AND IMPLANT FRACTURE.
Patient problems: Bone Fracture(s); No Code Available
MAUDE report 9493820 ↗
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 Screw, fixation, bone devices
- NA 03.043.029Synthes GmbH · Screw, fixation, bone503 reports
- OSTEORAPTOR 72201995Smith & Nephew, Inc. · Screw, fixation, bone253 reports
- Control 360 SK12Treace Medical Concepts, Inc. · Screw, Fixation, Bone195 reports
- HEALIX PEEK ORTHOCORD 222205Medos International Sàrl · Screw, fixation, bone186 reports
- PRECICE® Bone Transport System STP3.5-400Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-225Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-300Nuvasive Specialized Orthopedics, Inc. · Screw, 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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