LCP 04.112.009Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982102386), received between Feb 14, 2017 and Feb 14, 2017 — classified as 1 malfunction.

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

• MalfunctionFeb 14, 2017Break; Break

  DEVICE REPORT FROM SYNTHES ON AN EVENT IN (B)(6) AS FOLLOWS: IT WAS REPORTED THAT A LOCKING COMPRESSION PLATE BROKE WHILE BENDING IT WITH A BENDING PLIERS. THERE WAS NO PROLONGATION OF SURGERY REPORTED AND NO PATIENT HARM. COMPLAINT INVOLVES 1 PART. REPORTED CONCOMITANT DEVICES: BENDING PLIERS (PART / LOT: UNKNOWN, QUANTITY: 1. THIS REPORT IS 1 OF 1 FOR (B)(4).

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6330019 ↗