VA-LCP 02.211.255Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886982054562), received between Apr 10, 2024 and Apr 11, 2024 — classified as 2 injuries.

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryApr 11, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT ON AN UNKNOWN DATE THAT IN COLLABORATION WITH DEPUY SYNTHES, DR., TOGETHER WITH CLINIC (B)(6) DATABASE DESIGNERS, PROGRAM MANAGERS, RESEARCH ASSISTANTS, AND BIOSTATISTICIANS, HAS DEVELOPED A REPORT THAT SUMMARIZES SAFETY AND EFFECTIVENESS DATA ON 100 PATIENTS WHO UNDERWENT FOOT SURGERY AT (B)(6) BETWEEN 2008 AND 2023 UTILIZING DEPUY SYNTHES (DPS) FOOT PLATES. SOME PATIENTS WERE NOTED TO HAVE ADJUNCTIVE DEPUY SYNTHES DEVICES USED OUTSIDE OF THE PLATES/SCREWS. PATIENT #10 53-YEAR-OLD FEMALE WAS IMPLANTED WITH A VA LCP FOREFOOT/MIDFOOT PLATES (02.211.255) WITH 5 SCREWS. POST OP COMPLICATION WAS REPORTED FOR 1. SURGICAL WOUND DEHISCENCE, LEFT FOOT. 2. HEMATOMA, LEFT FOOT. THE COMPLICATION IS NOTED TO BE NOT RELATED TO THE PROCEDURE OR IMPLANTS. REHOSPITALIZATION WAS REQUIRED FOR 1. SURGICAL WOUND DEHISCENCE, LEFT FOOT. 2. HEMATOMA, LEFT FOOT. TREATMENT: 1. EVACUATION OF HEMATOMA, LEFT FOOT. 2. SECONDARY CLOSURE, SURGICAL WOUND, LEFT FOOT. 3. APPLICATION OF WOUND VAC, LEFT FOOT THIS REPORT IS FOR ONE (1) 2.4/2.7 VA-LCP T-FUSN PL 2 HOLE HD/LONG THIS IS REPORT 1 OF 6 FOR COMPLAINT (B)(4).

  Patient problems: Hematoma; Wound Dehiscence

  MAUDE report 19089370 ↗
• InjuryApr 10, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  FOOT PLATES: IN COLLABORATION WITH DEPUY SYNTHES, TOGETHER WITH CLEVELAND CLINIC FOUNDATION (CCF) DATABASE DESIGNERS, PROGRAM MANAGERS, RESEARCH ASSISTANTS, AND BIOSTATISTICIANS, HAS DEVELOPED A REPORT THAT SUMMARIZES SAFETY AND EFFECTIVENESS DATA ON 100 PATIENTS WHO UNDERWENT FOOT SURGERY AT CCF BETWEEN 2008 AND 2023 UTILIZING DEPUY SYNTHES (DPS) FOOT PLATES. SOME PATIENTS WERE NOTED TO HAVE ADJUNCTIVE DEPUY SYNTHES DEVICES USED OUTSIDE OF THE PLATES/SCREWS. PATIENT #5 27-YEAR-OLD FEMALE WAS IMPLANTED WITH A VA LCP FOREFOOT/MIDFOOT PLATES (02.211.255) WITH 4 SCREWS. ONE ADDITIONAL ADJUNCTIVE FIXATION SCREWS WAS USED FOR FRACTURE FIXATION - INTERMETATARSAL JOINT. POST OP COMPLICATION WAS REPORTED FOR PAINFUL HARDWARE, RIGHT FOOT; BUT FRACTURE HEALED. THE COMPLICATION IS NOTED TO BE RELATED TO THE PROCEDURE OR IMPLANTS. THERE IS NO DEVICE FAILURE NOTED. TREATMENT: DEEP IMPLANT REMOVAL, RIGHT FOOT. THIS REPORT IS FOR A 2.4/2.7MM VA-LCP T-FUSION PL 2 HOLE HEAD/LONG. THIS IS REPORT 1 OF 5 FOR (B)(4).

  Patient problems: Pain

  MAUDE report 19083416 ↗