ADVANCE® KIMP514LRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M684KIMP514L1), received between Jun 7, 2019 and Nov 17, 2020 — classified as 2 injuries.

The most frequently reported specific device problem is “Unstable” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryNov 17, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ALLEGEDLY, PATELLA RESURFACING AND POLY SWAP , SAME THICKNESS POLY WAS PUT BACK IN . LEFT KNEE COMPONENTS NOT REVISED: ADVANCE® PRIMARY FEMORAL SIZE 5 LEFT POROUS PRODUCT ID : KFTCPC5L LOT NUMBER: 01333763, ADVANCE® II SPIKED TIBIAL BASE POROUS COATED SIZE 5+ PRODUCT ID: KTSPPC51 LOT NUMBER : 09227685, ADVANCE® MODULAR KEEL SZ 5/6 PRODUCT ID: SPKT0024 LOT NUMBER: 01334085.

  Patient problems: Not Applicable

  MAUDE report 10851708 ↗
• InjuryJun 7, 2019Unstable; Unstable

  ALLEGEDLY THE PATIENT WAS REVISED DUE TO INSTABILITY. (RIGHT).

  Patient problems: No Information

  MAUDE report 8679987 ↗