Zimmer® Natural Nail® System 47-2493-212-10Recalls & reported problems
Zimmer GmbH · ZNN CMN NAIL 10MMX21.5CM 130R · 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
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024298910), received between Aug 5, 2020 and Feb 24, 2026 — classified as 4 injuries.
The most frequently reported specific device problem is “Fracture” (3 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.
Reports received per month
Most reported problems
Device problems
- Fracture3
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Nonunion/Delayed-union Bone Fracture2
- Pain2
- Ambulation or Postural Difficulties1
- Bone Fracture(s)1
- Failure of Implant1
- Insufficient Information1
- No Code Available1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryFeb 24, 2026Fracture
DILIGENCE IS COMPLETED AND NO FURTHER INFORMATION ON THE REPORTED EVENT HAS BEEN PROVIDED.
Patient problems: Insufficient Information; Nonunion/Delayed-union Bone Fracture
MAUDE report 24428925 ↗InjuryJun 17, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PATIENT HAD A REVISION SURGERY APPROXIMATELY ONE (1) YEAR AFTER IMPLANTATION DUE TO PAIN AND PSEUDOARTHROSIS. THE NAIL WAS REMOVED WITHOUT DIFFICULTY, AND A TOTAL HIP ARTHROPLASTY WAS PERFORMED WITHOUT COMPLICATIONS. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Nonunion/Delayed-union Bone Fracture; Pain
MAUDE report 19548445 ↗InjuryAug 20, 2021Fracture; Fracture
PATIENT WAS IMPLANTED ON THE RIGHT SIDE AND UNDERWENT A REVISION SURGERY DUE TO IMPLANT FRACTURE. FOLLOWING A MISSTEP AROUND JUN 15, THE PATIENT EXPERIENCED SEVERE PAIN AND COULD NO LONGER WALK.
Patient problems: Ambulation or Postural Difficulties; Bone Fracture(s); Failure of Implant; Pain
MAUDE report 12347397 ↗InjuryAug 5, 2020Fracture; Fracture
PATIENT WAS IMPLANTED ON THE RIGHT SIDE AND UNDERWENT REVISION SURGERY DUE TO IMPLANT FRACTURE. REASON FOR FRACTURE IS UNKNOWN.
Patient problems: No Code Available
MAUDE report 10367331 ↗
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- 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
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- 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.
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