ADVANCE® KIMP510RRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M684KIMP510R1), received between Jun 25, 2019 and Jun 23, 2020 — classified as 2 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJun 23, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  ALLEGEDLY, PATIENT WAS REVISED DUE TO STIFFNESS. COMPONENTS NOT REVISED: ADVANCE II COCR TIBIA BASE NONPOROUS SZ 5 STANDARD PRODUCT ID: KTCCNP50 LOT ID: 087465508. ADVANCE ONLAY ALL POLY PATELLA 38MM TRIPEG PRODUCT ID: KPONTP38 PRODUCT ID: 046332811. REVISION NJR NUMBER: 1058353. SIDE: R. PRIMARY ASA: P3 - INCAPACITATING SYSTEMIC DISEASE.

  Patient problems: Loss of Range of Motion

  MAUDE report 10184526 ↗
• InjuryJun 25, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

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

  Patient problems: Loss of Range of Motion

  MAUDE report 8732928 ↗