Zimmer® Natural Nail® System 47-2485-115-10Recalls & reported problems
Zimmer GmbH · ZNN CMN LAG SCREW 10.5X115 · 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 00889024298484), received between Mar 24, 2019 and Apr 20, 2023 — classified as 3 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
- Misassembly by Users1
- Patient Device Interaction Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Code Available1
- Nonunion/Delayed-union Bone Fracture1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryApr 20, 2023Misassembly by Users; Misassembly by Users
IT WAS REPORTED THAT A PATIENT UNDERWENT A PROCEDURE FOR A PERTROCHANTERIC FRACTURE WITH A NAIL. POST-OP X-RAYS SHOWED THE CERVICAL SCREW AND THE TWO DISTAL SCREWS HAD PASSED ABOVE THE NAIL, AND NOT PASSED THROUGH THE HOLES PROVIDED IN THE NAIL. THE NAIL WAS REMOVED AND REPLACED. DUE DILIGENCE IS IN PROGRESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION OR PRODUCT HAS BEEN RECEIVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16774595 ↗InjuryJul 13, 2022Patient Device Interaction Problem; Patient Device Interaction Problem
IT WAS REPORTED THAT THE FRACTURE ON THE RIGHT HIP FAILED TO HEAL. ABOUT 1,5 MONTHS AFTER THE IMPLANTATION, THE PATIENT UNDERWENT REVISION SURGERY. DUE DILIGENCE IS IN PROGRESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION OR PRODUCT HAS BEEN RECEIVED.
Patient problems: Nonunion/Delayed-union Bone Fracture
MAUDE report 14998933 ↗InjuryMar 24, 2019Fracture; Fracture
PLEASE REFER TO REPORT 0009613350-2019-00159.
Patient problems: No Code Available
MAUDE report 8446673 ↗
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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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