Medial Rotation Knee 156-513Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05055455503717), received between Apr 18, 2019 and Apr 18, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 18, 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.

• MalfunctionApr 18, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

  "REVISION LEFT KNEE (MRK), POLY LINERS AND RESURFACING PATELLA." "OPERATION DATE: (B)(6) 2019. PATIENT HAS THE FOLLOWING IMPLANTS: FEMUR SIZE 2, TIBIA SIZE 1, 13MM POLY, 20MM PATELLA. PATIENT WAS ORIGINALLY DONE BY MR. (B)(6) AT (B)(6) HOSPITAL ON (B)(6) 2006." REVISION LEFT KNEE (MRK), POLY LINERS AND RESURFACING PATELLA." (B)(4).

  Patient problems: Patient Problem/Medical Problem

  MAUDE report 8526375 ↗