LCP 224.754Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982158680), received between Aug 26, 2024 and Aug 26, 2024 — 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. 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.

• InjuryAug 26, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  SUBJECT (B)(6). IT WAS REPORTED THAT A CLINICAL ADVERSE EVENT WAS RECEIVED FOR LOSS OF FRACTURE REDUCTION TREATMENT/IMPACT: RECOMMENDED FOLLOW-UP WITH PLASTIC SURGERY AND INFECTIOUS DISEASE. RECOMMEND CONTINUED USE OF TELFA AND SILVADENE DRESSINGS OVER THE HEALING WOUNDS. THE PATIENT WILL REMAIN NON-WEIGHTBEARING OF THE LEFT LOWER EXTREMITY. THIS REPORT IS FOR ONE (1) 4.5MM/3.5MM LCP® METAPHYSEAL PLATE 9 HOLES. THIS IS REPORT 1 OF 2 FOR COMPLAINT (B)(4).

  Patient problems: Nonunion/Delayed-union Bone Fracture

  MAUDE report 20066267 ↗