Zimmer® Natural Nail® System 47-2485-120-10Recalls & reported problems
Zimmer GmbH · ZNN CMN LAG SCREW 10.5X120 · 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 00889024298491), received between Dec 17, 2019 and Oct 3, 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 problems
- Failure of Implant2
- No Code Available1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryOct 3, 2022Migration or Expulsion of Device; Migration or Expulsion of Device
IT WAS REPORTED THAT A PATIENT UNDERWENT A PROCEDURE TO REPAIR A LEFT, COMMINUTED, SUBTROCHANTERIC FRACTURE. ON AN UNKNOWN TIMEFRAME POST-IMPLANTATION, THE CONNECTION BETWEEN THE TITANIUM ROD OF THE FEMUR AND THE SCREW SPINDLE OF THE JOINT HEAD LOOSENED AND SHIFTED. THE FRACTURE HAS NOT HEALED DUE TO THE LOOSENING AND CONSTANT MOVEMENTS. ADDITIONAL SURGERY IS PENDING. DUE DILIGENCE IS IN PROGRESS FOR THIS EVENT; TO DATE NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Failure of Implant
MAUDE report 15526764 ↗InjuryOct 6, 2020Fracture; Fracture
InjuryDec 17, 2019Fracture; Fracture
PLEASE REFER TO REPORT 0009613350-2019-00805.
Patient problems: Failure of Implant
MAUDE report 9480933 ↗
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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 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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