LC-DCP 449.926Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982224460), received between Jul 17, 2018 and Jul 17, 2018 — 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. 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.

• InjuryJul 17, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT UNDERWENT AN IMPLANT PROCEDURE ON AN UNKNOWN DATE APPROXIMATELY COUPLE OF MONTHS PRIOR TO (B)(6) 2018. ON (B)(6) 2018, PATIENT UNDERWENT HARDWARE REMOVAL DUE TO NONUNION. THE SURGEON REMOVED ONE (1) TITANIUM LIMITED CONTACT DYNAMIC COMPRESSION PLATE (LC-DCP) AND SIX (6) CORTEX SCREWS OF VARYING LENGTHS. NO DIRECT BONE HEALING WAS NOTED. ADDITIONAL MEDICAL INTERVENTION INCLUDED PINNING OF THE FINGER. REPORTEDLY, THIS WAS A THIRD SURGERY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. THE (B)(4) WILL CAPTURE INTRAOPERATIVE EVENT OCCURRED DURING REMOVAL. THIS (B)(4) CAPTURES POST-OPERATIVE NON-UNION. THIS REPORT IS FOR ONE (1) 2.4MM TI LC-DCP® PLATE 6 HOLES/47MM. THIS IS REPORT 1 OF 7 FOR (B)(4).

  Patient problems: No Code Available; Nonunion/Delayed-union Bone Fracture

  MAUDE report 7695571 ↗