LCP 02.110.105Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982030283), received between Oct 28, 2025 and Oct 28, 2025 — classified as 1 injury.

1 other recall cover devices cleared under the same FDA submission (K070946); they may or may not involve this specific model.

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.

• InjuryOct 28, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION ORIF ABOVE EXISTING THE PLATE. THERE WAS A FRACTURE ABOVE THE EXISTING PLATE.

  Patient problems: Bone Fracture(s)

  MAUDE report 23402505 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K070946. One submission often covers many models, so check the product and lot details in each record.

• Z-1949-2016 · May 2, 2016 · Terminated
  LCP Dia-Meta Volar Distal Radius Plate 15 H Shaft/LT-Sterile; Indicated for fractures, osteotomies, and non-unions of the radius and other small bones.