LCP 02.110.007Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982030191), received between May 24, 2018 and May 24, 2018 — 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 18, 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.

• InjuryMay 24, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT ON (B)(6) 2018, THE PATIENT HAD A PAINFUL HARDWARE REMOVAL OF THE WRIST. IT WAS UNKNOWN WHY THE PATIENT WANTED THE HARDWARE OUT OTHER THAN IT WAS PAINFUL. THERE WERE EIGHT (8) UNKNOWN SCREWS, FOUR (4) UNKNOWN LOCKING SCREWS, FOUR (4) UNKNOWN CORTEX SCREWS AND A DIA-META VOLAR DISTAL RADIUS PLATE THAT WERE REMOVED INTACT. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH WAS NO SURGICAL DELAY. PATIENT OUTCOME IS UNKNOWN. THIS REPORT IS FOR A LCP DIA-META VOLAR DISTAL RADIUS PL 7H SHAFT/RT. THIS IS REPORT 1 OF 4 FOR (B)(4).

  Patient problems: Pain

  MAUDE report 7542166 ↗

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.