NCB® 02.03260.113Recalls & reported problems
Zimmer GmbH · NCB PLATE FOR FEMUR, LEFT, 13 HOLES · Class 2
Data updated Oct 13, 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 00889024297418), received between Dec 6, 2021 and Apr 22, 2025 — classified as 5 injuries.
The most frequently reported specific device problem is “Fracture” (4 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
- Fracture4
- Material Integrity Problem2
- Patient Device Interaction Problem1
Patient problems
- Failure of Implant5
- Nonunion/Delayed-union Bone Fracture2
- Pain2
- Bone Fracture(s)1
- Crepitus1
- Necrosis1
- Swelling/ Edema1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryApr 22, 2025Fracture; Fracture
IT WAS REPORTED THAT THE PATIENT HAD AN INITIAL SURGERY WITH AN NCB PLATE. SUBSEQUENTLY, EXPERIENCED EXTREME SWELLING IN HER LEFT THIGH AND A FRACTURE OF THE PLATE WAS DISCOVERED DURING X-RAY DIAGNOSTICS. IT IS UNKNOWN IF REVISION SURGERY IS PLANNED OR WAS PERFORMED. DILIGENCE IS COMPLETED AND NO FURTHER INFORMATION ON THE REPORTED EVENT HAS BEEN PROVIDED.
Patient problems: Crepitus; Failure of Implant; Necrosis; Pain; Swelling/ Edema
MAUDE report 21883720 ↗InjuryMay 23, 2024Fracture; Fracture
DILIGENCE IS COMPLETED AND NO FURTHER INFORMATION ON THE REPORTED EVENT HAVE BEEN PROVIDED
Patient problems: Failure of Implant; Nonunion/Delayed-union Bone Fracture; Pain
MAUDE report 19382744 ↗InjuryJul 14, 2023Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Failure of Implant
MAUDE report 17323169 ↗InjuryMar 28, 2022Fracture; Material Integrity Problem; Fracture; Material Integrity Problem
IT WAS REPORTED THAT THE PATIENT HAD A REVISION DUE TO IMPLANT FRACTURE.
Patient problems: Bone Fracture(s); Failure of Implant
MAUDE report 13927578 ↗InjuryDec 6, 2021Material Integrity Problem; Patient Device Interaction Problem; Material Integrity Problem; Patient Device Interaction Problem
IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED DUE TO IMPLANT FRACTURE AND NON UNION.
Patient problems: Failure of Implant; Nonunion/Delayed-union Bone Fracture
MAUDE report 12934191 ↗
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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.
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