LCP 02.112.091Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982033239), received between Oct 4, 2019 and Oct 4, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Use of Device Problem” (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.

• MalfunctionOct 4, 2019Use of Device Problem; Use of Device Problem

  IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE PATIENT UNDERWENT AN UNKNOWN PROCEDURE. WHILE THE SURGEON WAS OPERATING ON A RIGHT CLAVICLE, IT WAS FOUND OUT NEAR THE END OF THE CASE THAT A LOCKING COMPRESSION PLATE (LCP) CLAVICLE PLATE WITH LATERAL EXTENSION WAS A LEFT. IT WAS ALSO REPORTED THAT THE SURGEON WAS INFORMED IMMEDIATELY BY THE SALES CONSULTANT. IT WAS MENTIONED THAT THERE WAS NO ISSUE ON THE PACKAGING OF LABELING. IT WAS IMPROPER IMPLANT SELECTION. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH NO SURGICAL DELAY. THE PATIENT OUTCOME IS UNKNOWN. THIS IS REPORT 1 FOR 1 (B)(4).

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9156558 ↗