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PHOENIX NAIL SYSTEM 14-405024Recalls & reported problems

Biomet Orthopedics, LLC · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887868092480), received between Nov 21, 2025 and Nov 21, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Biocompatibility” (1 report).

5 other recalls cover devices cleared under the same FDA submission (K050118, K063570); they may or may not involve this specific model.

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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 1 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Biocompatibility1

Patient problems

  • Hypersensitivity/Allergic reaction1
  • Rash1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryNov 21, 2025Biocompatibility; Biocompatibility

    IT WAS REPORTED THAT A PATIENT HAD AN INITIAL PLATE AND NAIL SYSTEM PROCEDURE. THREE MONTHS POSTOPERATIVELY, ECZEMA DEVELOPED AROUND THE SURGICAL SITE, RAISING SUSPICION OF METAL ALLERGY. CONSEQUENTLY, ALL IMPLANTS WERE REMOVED. THE PATIENT IS LIKELY A POTENTIAL CARRIER OF METAL ALLERGIES. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

    Patient problems: Hypersensitivity/Allergic reaction; Rash

    MAUDE report 23618011 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K050118, K063570. One submission often covers many models, so check the product and lot details in each record.

  • Z-0625-2021 · Nov 25, 2020 · Terminated
    PHOENIX, Interlocking screw for IM nail, Item numbers 14-405040, 14-405042, 14-405044, 14-405070 - Product Usage: Fracture fixation of small bones, small bone fragements and long b
  • Z-0627-2021 · Nov 25, 2020 · Terminated
    RINGLOC ACETABULAR SYSTEM Self-tapping bone screws, Item numbers 103531, 103533, 103534, 103535 - Product Usage: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented; Prosthe
  • Z-1819-2016 · Apr 1, 2016 · Terminated
    Various trauma and sports medicine instruments and implants. Rod, fixation, intramedullary and accessories.
  • Z-1478-2012 · Mar 30, 2012 · Terminated
    REF 28234 Troch Nail, Long 11MM, Right 34 CM Peritrochanteric Nail System, Rx Sterile Biomet Trauma Persippany, NJ Rod, Fixation, Intramedullary and Accessories Product Usage: An
  • Z-0012-06 · Jun 24, 2005 · Terminated
    EBI Trochanteric 11mm Long Nail.

Other ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices

All ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page