LCP 04.110.150Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886982100320), received between Aug 6, 2019 and Aug 12, 2019 — classified as 2 injuries.

The most frequently reported specific device problem is “Migration” (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. 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.

• InjuryAug 12, 2019Migration; Migration

  IT WAS REPORTED THAT ON (B)(6) 2019, PATIENT UNDERWENT REMOVAL OF ONE (1) TITANIUM LOCKING COMPRESSION PLATE (LCP) WRIST FUSION STANDARD BEND PLATE AND EIGHT (8) UNKNOWN LOCKING SCREWS. THERE WAS A FAILURE OF THE LOCKING SCREWS OVER THE 3RD METACARPAL. THE SCREWS HAD FAILED AT THE HEAD SHAFT JUNCTION. THE METAL PLATE HAD LIFTED ITSELF OFF THE 3RD METACARPAL AND WAS PROMINENT OVER THE DORSAL ASPECT OF THE RIGHT HAND AND FOUR (4) UNKNOWN LOCKING SCREWS WERE BROKEN. EXTENSIVE ADHESIONS WERE PRESENT BETWEEN THE SUBCUTANEOUS TISSUES AND EXTENSOR TENDONS. A SWELLING AND PROMINENCE WERE NOTED OVER THE DORSAL ASPECT OF THE 3RD METACARPAL WHERE THE LCP STANDARD BEND PLATE HAD DISENGAGED FROM THE 3RD METACARPAL. THERE WAS NO SURGICAL DELAY. PROCEDURE OUTCOME WAS SUCCESSFUL. PATIENT STATUS IS UNKNOWN. CONCOMITANT DEVICE REPORTED: UNKNOWN LOCKING SCREWS (PART #: UNKNOWN, LOT #: UNKNOWN, QUANTITY #: 4). THIS IS REPORT 1 OF 5 FOR (B)(4).

  Patient problems: Arthritis; No Code Available; Swelling

  MAUDE report 8884258 ↗
• InjuryAug 6, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE VALLEY HEALTH MEDICAL CENTER FROM PATHOLOGY DEPARTMENT GOT A REPOSITION WITH INFORMATION FROM THE DOCTOR INVOLVED IN A CASE. A TITANIUM WRIST FUSION STANDARD BEND PLATE WAS REMOVED AND MUST GO TO THE COMPANY FOR ANALYSIS. IT IS UNKNOWN IF THERE WAS SURGICAL DELAY. PROCEDURE OUTCOME AND PATIENT STATUS WERE UNKNOWN. CONCOMITANT DEVICE REPORTED: UNK - SCREWS: TRAUMA (PART # UNKNOWN, LOT # UNKNOWN, QUANTITY # UNKNOWN). THIS COMPLAINT INVOLVES ONE (1) DEVICE. THIS REPORT IS 1 OF 1 FOR (B)(4).

  Patient problems: Failure of Implant; No Code Available

  MAUDE report 8866245 ↗