NCB® 02.03260.013Recalls & reported problems
Zimmer GmbH · NCB PLATE FOR FEMUR, RIGHT, 13 HOLES · Class 2
Data updated Oct 13, 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 00889024297388), received between Nov 19, 2019 and Jan 19, 2026 — classified as 8 injuries.
The most frequently reported specific device problem is “Fracture” (7 reports).
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture7
- Break1
Patient problems
- Failure of Implant6
- Insufficient Information1
- No Information1
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
InjuryJan 19, 2026Fracture
IT WAS REPORTED THAT THE PATIENT UNDERWENT REMOVAL OF A PLATE AND SCREWS APPROXIMATELY FIVE MONTHS POST-IMPLANTATION. PHOTOGRAPHS CONFIRM THAT THE PLATE HAD FRACTURED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Insufficient Information
MAUDE report 24108604 ↗InjuryFeb 27, 2025Fracture; Fracture
DILIGENCE IS COMPLETED AND NO FURTHER INFORMATION ON THE REPORTED EVENT HAS BEEN PROVIDED.
Patient problems: Failure of Implant
MAUDE report 21479449 ↗InjuryMar 30, 2023Break; Break
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Failure of Implant
MAUDE report 16643026 ↗InjuryAug 24, 2022Fracture; Fracture
IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION SURGERY DUE TO IMPLANT FRACTURE 12 WEEKS AFTER IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Failure of Implant
MAUDE report 15281010 ↗InjuryJun 15, 2022Fracture; Fracture
IT WAS REPORTED THAT THE PATIENT UNDERWENT A RIGHT IMPLANT REVISION APPROXIMATELY 6 MONTHS POST-OP DUE TO AN IMPLANT FRACTURE. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: Failure of Implant
MAUDE report 14692535 ↗InjuryJun 2, 2022Fracture; Fracture
IT WAS REPORTED THAT THE TRAUMA PLATE BROKE APPROXIMATELY 4 MONTHS AFTER IMPLANTATION AND REVISION SURGERY WAS PERFORMED. DUE DILIGENCE IS IN PROGRESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION OR PRODUCT HAS BEEN RECEIVED.
Patient problems: Failure of Implant
MAUDE report 14573196 ↗InjuryApr 19, 2022Fracture; Fracture
IT WAS REPORTED, THAT: THERE WAS A REVISION DUE TO IMPLANT BREAKAGE. PATIENT OUTCOME - REVISION DUE TO IMPLANT FRACTURE.
Patient problems: Failure of Implant
MAUDE report 14140001 ↗InjuryNov 19, 2019Fracture; Fracture
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 STP3.5-375Nuvasive 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 STP3.5-200Nuvasive 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 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