Skip to content

NEOFIX 900.927Recalls & reported problems

Neoortho Produtos Ortopédicos S/A. · 8-Holes 1.5 Straight Plate · Class 2

Data updated Oct 16, 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 07899893204038), received between May 3, 2017 and May 3, 2017 — classified as 1 injury.

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 16, 2026.

Most reported problems

Device problems

  • Fracture1
  • Improper or Incorrect Procedure or Method1

Patient problems

  • Nonunion/Delayed-union Bone Fracture1
  • Pain1

Recent adverse event reports

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

  • InjuryMay 3, 2017Fracture; Improper or Incorrect Procedure or Method; Fracture; Improper or Incorrect Procedure or Method

    PLATE BREAKAGE 900.927, LOT 3654981, 30 DAYS AFTER ITS IMPLANTATION. PATIENT: (B)(6) YEARS OLD - WITH PROXIMAL FLANGE FRACTURE OF THE 4TH FINGER OF THE RIGHT HAND, OPERATED ON (B)(6) 2017 AND PROGRESS TO PLATE BREAKAGE. PLATE REPLACEMENT SURGERY ON (B)(6) 2017. OTHER DEVICES USED: 903,240 LOT 3663832; 923.008 LOT 3663802; 923.009 LOT 3616173.

    Patient problems: Nonunion/Delayed-union Bone Fracture; Pain

    MAUDE report 6541984 ↗

Other Plate, Fixation, Bone devices

All Plate, Fixation, Bone devices →

Sources and updates

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