NA 237.86Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982161550), received between Sep 11, 2024 and Sep 11, 2024 — 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. How this data works · Data updated Oct 13, 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.

• InjurySep 11, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THIS COMPLAINT IS FROM A DATA USE AGREEMENT (DUA). THE DUA SUMMARIZES 64 PATIENTS THAT WERE IMPLANTED WITH ANGLED BLADE PLATES. IMPLANTATION WAS BETWEEN AUGUST 2000 TO JANUARY 2023 AT (B)(6). PATIENT NUMBER 17. PATIENT IS A 42-YEAR-OLD MALE. REASON FOR IMPLANTATION WAS PROXIMAL FEMUR FRACTURE FIXATION. POST OP COMPLICATION INCLUDED PAIN IN THIGH AND HIP DURING ACTIVITIES. TREATMENT/INTERVENTION INCLUDED REMOVAL OF BLADE PLATE AND SCREWS. IMPLANT(S) INVOLVED: 237.86 CONDYLAR PLATE 95°, 18HOLES, L 300MM, BLADE 80MM X1 CORTEX SCREW X6.

  Patient problems: Pain

  MAUDE report 20192327 ↗