LCP 223.410Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982157621), received between Feb 21, 2023 and Feb 21, 2023 — 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 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.

• InjuryFeb 21, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT ON AN UNKNOWN DATE, DURING POST-OP SALES CONSULTANT WAS NOTIFIED THAT SURGEON WAS GOING TO BE REMOVING A PLATE FROM A DISTAL FEMUR BECAUSE OF PAIN. THE HARDWARE WAS REMOVED SUCCESSFULLY. ADDITIONALLY, DURING THE REMOVAL, A SCREW DRIVER SHAFT FROM THE SCREW REMOVAL SET WAS NOTICED TO BE BENT. IT WAS DISCARDED AND A NEW ONE WILL BE PURCHASED BY THE HOSPITAL. THIS REPORT IS FOR ONE (1) 3.5MM LCP METAPHYSEAL PLATE 10 HOLES THIS IS REPORT 1 OF 12 FOR COMPLAINT (B)(4).

  Patient problems: Pain

  MAUDE report 16415111 ↗