ADVANCE® KIMP210RRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI M684KIMP210R1), received between Jun 29, 2020 and Aug 3, 2022 — classified as 3 injuries.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryAug 3, 2022Adverse Event Without Identified Device or Use Problem

  ALLEGEDLY, PATIENT WAS REVISED DUE TO INFECTION. REVISION NJR NUMBER: (B)(4). SIDE: R . PRIMARY ASA: P2 - MILD DISEASE NOT INCAPACITATING.

  Patient problems: Unspecified Infection

  MAUDE report 15156421 ↗
• InjuryApr 6, 2022Loss of Osseointegration; Loss of Osseointegration

  ALLEGEDLY, PATIENT WAS REVISED DUE TO ASEPTIC LOOSENING FEMUR/ASEPTIC LOOSENING TIBIA REVISION NJR NUMBER: (B)(4); SIDE: R ; PRIMARY ASA: P2 - MILD DISEASE NOT INCAPACITATING.

  Patient problems: Insufficient Information

  MAUDE report 14021052 ↗
• InjuryJun 29, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

  ALLEGEDLY, PATIENT WAS REVISED DUE TO COMPONENT DISSOCIATION. COMPONENTS NOT REVISED: ADVANCE STEMMED MEDIAL PIVOT NONPOROUS FEMORAL SIZE 2 RIGHT PRODUCT ID: KFSCNP2R LOT ID: 1416609. ADVANCE II MODULAR TITANIUM TIBIA BASE SZ 2 STD NONPOROUS PRODUCT ID: KTTINP20 LOT ID: 1633508. ADVANCE ONLAY ALL POLY PATELLA 35MM TRIPEG PRODUCT ID : KPONTP35 LOT ID:1683375. REVISION NJR NUMBER: 4440033. SIDE:R. PRIMARY ASA: P2 - MILD DISEASE NOT INCAPACITATING.

  Patient problems: No Information

  MAUDE report 10206493 ↗