LCP 226.652Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982159243), received between Jan 19, 2018 and Jan 19, 2018 — classified as 1 injury.

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

1 other recall cover devices cleared under the same FDA submission (K000682, K041911, K082807); 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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJan 19, 2018Break; Break

  IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION SURGERY DUE TO A BROKEN 4.5MM CURVED BROAD LCP PLATE ON (B)(6) 2017. THE PLATE, SEVEN (7) LOCKING SCREWS, TWO (2) 1.7MM CABLES AND THREE (3) 4.5MM THREADED POSITIONING PINS, WERE ORIGINALLY IMPLANTED ON (B)(6) 2017 DURING A PERIPROSTHETIC MIDSHAFT FEMUR FRACTURE PROCEDURE WITH KNEE STEM. DURING THE REVISION THE BROKEN PLATE, AND INTACT SCREWS, CABLES AND PINS WERE ALL REMOVED SUCCESSFULLY AND THE PATIENT WAS REVISED TO A NEW SET OF IMPLANTS. NO SURGICAL DELAY WAS REPORTED AND PATIENT WAS LISTED AS STABLE AFTER THE SURGERY. CONCOMITANT DEVICES REPORTED: PART # 212.202, LOT # UNKNOWN, QUANTITY # 1, PART # 212.212, LOT # UNKNOWN, QUANTITY # 1 , PART # 212.213, LOT # UNKNOWN, QUANTITY # 1 , PART # 212.214, LOT # UNKNOWN, QUANTITY # 3 , PART # 212.218, LOT # UNKNOWN , QUANTITY # 1 , PART # 298.801.01S, LOT # P269025, QUANTITY # 1 , PART # 298.801.01S, LOT # P276185, QUANTITY# 1 , PART # UNK - PINS/WIRES, LOT # UNKNOWN, QTY # 3. THIS REPORT IS 1 OF 1 FOR (B)(4).

  Patient problems: Failure of Implant

  MAUDE report 7206827 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K000682, K041911, K082807. One submission often covers many models, so check the product and lot details in each record.

• Z-0409-2014 · Jul 30, 2013 · Terminated
  Synthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing multifragmentary distal femur fractures.