LCP 224.753Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982158673), received between May 16, 2024 and May 16, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device-Device Incompatibility” (1 report).

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. How this data works · Data updated Oct 13, 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.

• MalfunctionMay 16, 2024Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT ON AN UNKNOWN DATE IN 2024 A METAPHYSEAL PLATE COULD NOT BE USED DUE TO LOCKING SCREW NOT LOCKING. SURGEON USED A DIFFERENT PLATE. THERE WAS NO SURGICAL DELAY. THERE WERE NO PATIENT OUTCOME. THIS REPORT IS FOR ONE (1) 4.5MM/3.5MM LCP® METAPHYSEAL PLATE 8 HOLES. THIS IS REPORT 1 OF 2 FOR COMPLAINT (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19337286 ↗