NA 237.24Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982161154), 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 (B)(6) 2000 TO (B)(6) 2023 AT (B)(6). PATIENT NUMBER 62. PATIENT IS A 36 YEARS OLD, FEMALE. REASON FOR IMPLANTATION WAS FRACTURE FIXATION. POST OP COMPLICATION INCLUDED SYMPTOMATIC HARDWARE - PAIN ALONG FEMUR ON LATERAL ASPECT WITH INABILITY TO LAY ON SIDE OF LEG. TREATMENT/INTERVENTION INCLUDED RHWR - REMOVAL OF BLADE PLATE AND SCREWS. IMPLANT(S) INVOLVED: 95 DEGREE 70MM. CORTEX SCREW X6. (B)(4) IS RELATED TO (B)(4) WHICH WAS CREATED TO CAPTURE THE PATIENT # 62. THIS REPORT IS FOR ONE (1) 95 DEG CONDYLAR PLATE 12 HOLES/70MM/204MM. THIS IS REPORT 1 OF 2 FOR COMPLAINT (B)(4)

  Patient problems: Pain

  MAUDE report 20193230 ↗