VA-LCP 02.211.254Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886982054548), received between Aug 29, 2019 and Apr 8, 2021 — 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 8, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE PATIENT UNDERWENT REMOVAL SURGERY DUE TO NON-UNION. TWO (2) 2.4/2.7MM PLATES AND ONE (1) UNKNOWN SCREW WERE REMOVED. THE PROCEDURE SUCCESSFULLY COMPLETED. NO PATIENT CONSEQUENCES. THIS REPORT IS FOR ONE (1) 2.4/2.7MM VA-LCP T-FUSION PL 2 HOLE HEAD/STANDARD. THIS IS REPORT 2 OF 3 FOR (B)(4).

  Patient problems: Nonunion/Delayed-union Bone Fracture

  MAUDE report 11639431 ↗
• InjuryAug 29, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT ON (B)(6) 2019, THE PATIENT UNDERWENT REMOVAL OF HARDWARE DUE TO PAIN CAUSED BY IMPINGEMENT, THE FOREFOOT MIDFOOT PLATE TOGETHER WITH SEVEN (7) UNKNOWN SCREWS (3 CORTEX AND 4 LOCKING SCREWS) WERE REMOVED. INITIALLY, THE PATIENT HAD A PREVIOUS FUSION WITH THE PLATE AND SCREWS ON AN UNKNOWN DATE. THERE WAS NO PATIENT CONSEQUENCE REPORTED. THIS IS REPORT 3 OF 8 FOR (B)(4).

  Patient problems: No Code Available; Pain

  MAUDE report 8945090 ↗