Zimmer® Natural Nail® System 47-2485-110-10Recalls & reported problems
Zimmer GmbH · ZNN CMN LAG SCREW 10.5X110 · Class 2 · Implant
All models of Zimmer Natural Nail System (57)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889024298477), received between Jul 11, 2019 and Mar 15, 2022 — classified as 3 injuries.
The most frequently reported specific device problem is “Fracture” (2 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Fracture2
- Migration or Expulsion of Device1
- Patient Device Interaction Problem1
Patient problems
- No Consequences Or Impact To Patient2
- Bone Fracture(s)1
- Pain1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryMar 15, 2022Migration or Expulsion of Device; Patient Device Interaction Problem; Migration or Expulsion of Device; Patient Device Interaction Problem
MIGRATION OF THE NAIL DISCOVERED ON 08/30/2021, A LOT OF PAIN + FEMORAL PSEUDARTHROSIS (FEMORAL NONUNION).
Patient problems: Bone Fracture(s); Pain
MAUDE report 13769477 ↗InjuryAug 22, 2019Fracture; Fracture
WHEN THE SURGEON TRIED TO PLACE THE LAG SCREW, THE TABS FRACTURED DUE TO THE DENSE BONE. THE PATIENT DID NOT RETAIN A FOREIGN DEVICE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8919643 ↗InjuryJul 11, 2019Fracture; Fracture
PLEASE REFER TO REPORT 0009613350-2019-00439.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8779506 ↗
Other ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices
- NA 03.033.001Synthes GmbH · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES265 reports
- GAMMA 3125-1180SStryker GmbH · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES249 reports
- NA 03.037.026Synthes GmbH · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES225 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-075Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls2 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-045Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls1 report
- PRECICE® Intramedullary Limb Lengthening System LSC5-050Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls1 report
- TRIGEN 71674067Smith & Nephew, Inc. · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES201 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-040Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 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