ADVANCE® KPRC25LORecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI M684KPRC25LO1), received between Mar 16, 2020 and Jul 5, 2023 — classified as 3 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (2 reports).

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.

• InjuryJul 5, 2023Insufficient Device Problem Information; Insufficient Device Problem Information

  ALLEGEDLY, PATIENT UNDERWENT R TKR ON (B)(6) 2019. REVISED ON (B)(6) 2023 DUE TO ANTERIOR PAIN. ADVANCE RECESSED ALL-POLY PATELLA REPLACED WITH ADVANCE ONLAY ALL-POLY PATELLA. AUSTRALIA-C23-229.

  Patient problems: Pain

  MAUDE report 17255518 ↗
• InjuryMar 16, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  ALLEGEDLY, PATIENT WAS REVISED DUE TO KNEE STIFFNESS, ALL MICROPORT IMPLANTS WERE REMOVE AND REPLACED WITH ANOTHER MANUFACTURER COMPANY. (B)(6).

  Patient problems: Loss of Range of Motion

  MAUDE report 9835322 ↗
• InjuryMar 16, 2020Malposition of Device; Malposition of Device

  ALLEGEDLY, PATIENT WAS REVISED DUE TO THE PATELLA IS NOT SITTING FLUSH WITH THE BONE , IT WAS REMOVED AND REPLACE WITH ANOTHER COMPANY'S PATELLA. (B)(6). PRODUCTS NOR REVISED: ADVANCE® BIOFOAM® TIBIA BASE W/ SCREWHOLES SIZE 4+ PRODUCT ID: KTSCFM41, LOT ID: 1507186. ADVANCE® PRESS FIT KEEL PRIMARY 15MM X SIZE 4+/5/5+ PRODUCT ID: KSPP1556, LOT ID: 1643668. CANCELLOUS BONE SCREW 6.5MM X 20M X 2 PRODUCT ID: 7552002000, LOT ID'S: 1664710 AND 1702907. ADVANCE® PRIMARY FEMORAL SIZE 4 RIGHT POROUS PRODUCT ID: KFTCPC4R, LOT ID: 1666205. ADVANCE® DOUBLE HIGH TIBIAL INSERT SZ 4 RIGHT 17MM PRODUCT ID: KIDH417R, LOT ID: 0285418821639748.

  Patient problems: No Information

  MAUDE report 9835140 ↗