LCB 00-1200-1002Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00841132109717), received between Mar 23, 2018 and Sep 15, 2026 — classified as 3 injuries, 3 malfunctions.

The most frequently reported specific device problem is “Fracture” (5 reports).

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 16, 2026.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjurySep 15, 2026Fracture

  The patient underwent surgery on (b)(6) 2026, during which bilateral 3.5 mm Blade Plates were used. Subsequently, one of the plates was reported to have fractured and was replaced with an LPF.

  Patient problems: Failure of Implant

  MAUDE report 50778280 ↗
• MalfunctionOct 24, 2025Fracture; Fracture

  DR. (B)(6) FROM (B)(6) HOSPITAL REPORTED A POST-OPERATIVE ISSUE INVOLVING A TRAUMA & DEFORMITY SYSTEM, SPECIFICALLY AN LCB BLADE PLATE (PART NUMBER: 00-1200-1002, LOT NUMBER: 241069-B), WHICH HAD BEEN IN USE FOR LESS THAN SIX MONTHS. THE DEVICE WAS IMPLANTED IN AN 8-YEAR-OLD FEMALE PATIENT (INITIALS (B)(6)) ON (B)(6) 2025 AND WAS REMOVED ON (B)(6) 2025, AFTER THE PLATE BROKE. THE ISSUE WAS DISCOVERED DURING A CLINIC VISIT POST-OPERATION. THE BROKEN DEVICE WAS SCRAPPED AND NOT RETURNED FOR EVALUATION.

  Patient problems: Failure of Implant

  MAUDE report 23380666 ↗
• MalfunctionOct 27, 2024Fracture; Fracture

  BLADE PLATE BROKEN SEEN BY XRAY AND DISCOMFORT BY PATIENT.

  Patient problems: Failure of Implant

  MAUDE report 20541654 ↗
• MalfunctionOct 27, 2024Fracture; Fracture

  INFANT BLADE PLATE BROKEN AT OSTEOTOMY LEVEL.

  Patient problems: Failure of Implant

  MAUDE report 20541652 ↗
• InjuryFeb 18, 2020Fracture; Fracture

  IT HAS BEEN REPORTED THAT APPROXIMATELY FOUR WEEKS FOLLOWING THE PLACEMENT OF A LOCKING CANNULATED BLADE PLATE, THE PATIENT UNDERWENT A REVISION DUE TO PLATE FRACTURE. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED.

  Patient problems: No Information

  MAUDE report 9720942 ↗
• InjuryMar 23, 2018Bent; Bent

  IT HAS BEEN REPORTED THAT FOLLOWING THE CLOSE OF A DEROTATIONAL OSTEOTOMY PROCEDURE, THE INFANT LOCKING CANNULATED BLADE PLATE WAS FOUND, VIA X-RAY, TO BE BENT. THE PATIENT WAS RE-OPENED AND THE INFANT BLADE PLATE REPLACED WITH A CHILD BLADE PLATE. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7366633 ↗

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-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-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-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