LCP 02.112.136Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982033857), received between Jan 22, 2018 and Jan 22, 2018 — classified as 1 injury.

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.

• InjuryJan 22, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED ON (B)(6) 2017 THAT HARDWARE REMOVAL WAS PERFORMED DUE TO SOFT TISSUE IRRITATION. ONE 3.5MM LCP T-PLATE 4H HEAD/4H SHAFT/56MM-RIGHT ANGLE, ONE 2.7MM/3.5MM LCP LATERAL DISTAL FIBULA PLATE 3H/RIGHT/73MM, EIGHT 3.5MM CORTEX SCREWS, ONE 3.5MM LOCKING SCREW, AND FOUR 2.7MM LOCKING SCREWS WERE REMOVED. INITIAL SURGERY WAS IN (B)(6) 2017 BUT ACTUAL DAY IS UNKNOWN. ALL PARTS WERE REMOVED WITHOUT ANY ISSUES AND INTACT. REMOVAL SURGERY WAS COMPLETED SUCCESSFULLY WITHOUT ANY NEW IMPLANTATION AND PATIENT STATUS WAS SATISFACTORY. THIS COMPLAINT INVOLVES 5 PARTS. THIS REPORT IS 2 OF 5 FOR (B)(4).

  Patient problems: Irritation; No Code Available

  MAUDE report 7210324 ↗