LCB 00-1200-5000Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841132110287), received between Feb 9, 2026 and Feb 9, 2026 — classified as 1 malfunction.

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

3 other recalls cover devices cleared under the same FDA submission (K110959, K260323); 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.

Most reported problems

Recent adverse event reports

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

• MalfunctionFeb 9, 2026Fracture

  PATIENT CAME TO THE HOSPITAL WITH SEVERE PAIN, DOCTOR SENT FOR XRAY AND AT THIS POINT DISCOVERED THAT THE PLATE WAS BROKEN INSIDE.

  Patient problems: Pain

  MAUDE report 24292456 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K110959, K260323. One submission often covers many models, so check the product and lot details in each record.

• Z-1535-2013 · Apr 19, 2013 · Terminated
  90 Degree Cannulated Infant Blade Plate 30mm x 5mm x 3 Hole Product Usage: The OrthoPediatrics Locking Cannulated Blade Plate System is intended for fixation of long bone fractur
• Z-1536-2013 · Apr 19, 2013 · Terminated
  90 Degree Cannulated Infant Blade Plate 35mm x 5mm x 3 Hole Product Usage: The OrthoPediatrics Locking Cannulated Blade Plate System is intended for fixation of long bone fractur
• Z-1534-2013 · Apr 19, 2013 · Terminated
  90 Degree Cannulated Infant Blade Plate 25mm x 5mm x 3 Hole Product Usage: The OrthoPediatrics Locking Cannulated Blade Plate System is intended for fixation of long bone fractur