LCP 426.611Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982217219), received between Dec 2, 2021 and Dec 2, 2021 — 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.

• InjuryDec 2, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT ON (B)(6) 2021, THE PATIENT UNDERWENT TOTAL KNEE EXPLANT, ONE (1) LOCKING COMPRESSION PLATE AND TEN (10) CORTEX SCREWS WERE REMOVED BECAUSE OF INFECTION. A ZIMMER BIOMET WAS ALSO PLANNED TO BE REMOVED BUT WAS UNSUCCESSFUL. THE SURGERY WAS COMPLETED SUCCESSFULLY WITHOUT A SURGICAL DELAY. THE PATIENT OUTCOME WAS GOOD. THIS COMPLAINT INVOLVES ELEVEN (11) DEVICES. THIS REPORT IS FOR (1) 4.5MM TI BROAD LCP® PLATE 11 HOLES/206MM. THIS IS REPORT 1 OF 11 FOR COMPLAINT (B)(4).

  Patient problems: Unspecified Infection

  MAUDE report 12920742 ↗