Zimmer® Natural Nail® System 47-2485-080-10Recalls & reported problems
Zimmer GmbH · ZNN CMN LAG SCREW 10.5X80 · 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
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024298415), received between Jul 28, 2020 and Sep 14, 2020 — classified as 2 injuries.
The most frequently reported specific device problem is “Fracture” (1 report).
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
- Fracture1
- Mechanical Jam1
Patient problems
- No Code Available2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjurySep 14, 2020Mechanical Jam; Mechanical Jam
DURING SURGERY IT WAS NOTICED BY THE SURGEON THAT THE SET SCREW WAS STUCK AND COULD NOT BE MOVED IN ANY DIRECTION. PRODUCT REMAINS IMPLANTED IN THE PATIENT. THE WHOLE PROCEDURE WAS DELAYED BY 60 MINUTES.
Patient problems: No Code Available
MAUDE report 10527500 ↗InjuryJul 28, 2020Fracture; Fracture
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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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