ATTUNE 1517-10-720Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10603295056195), received between Oct 6, 2020 and Apr 30, 2026 — classified as 8 injuries.

The most frequently reported specific device problem is “Unintended Movement” (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 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• InjuryApr 30, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT FELL AND NEEDED A DISTAL FEMORAL REPLACEMENT (DFR). DOI- UNKNOWN. DOR- (B)(6) 2026. AFFECTED SIDE-RIGHT KNEE.

  Patient problems: Fall

  MAUDE report 25046419 ↗
• InjuryNov 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THERE WAS REMOVAL TOTAL KNEE DUE TO INFECTION STAGE 1. AFFECTED SIDE: LEFT KNEE.

  Patient problems: Unspecified Infection

  MAUDE report 23467082 ↗
• InjuryAug 28, 2025Unintended Movement; Unintended Movement

  IT WAS REPORTED THAT THE PATIENT SPUN OUT OF RP POLY, PATIENT ALREADY HAD A SIZE 20 INSERT IN THERE. SINCE THE 26 DIDN'T WORK THEY HAD TO DO A HINGE FOR PATIENT. DOI: UNKNOWN. DOR: UNKNOWN. AFFECTED SIDE: RIGHT SIDE.

  Patient problems: Insufficient Information

  MAUDE report 22917920 ↗
• InjuryJun 10, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY THE DOCTOR THAT THE PATIENT WAS EXPERIENCING A LITTLE KNEE PAIN AND DECIDED TO DO A CLEAN OUT OF SOFT TISSUE AND POLY SWAP. THE PATIENT WENT BACK IN WITH THE SAME POLY SIZE AND SAID NOTHING LOOKED WRONG WITH THE IMPLANTS. DOI: (B)(6) 2024, DOR: (B)(6) 2025. AFFECTED AREA: RIGHT KNEE.

  Patient problems: Adhesion(s); Pain

  MAUDE report 22178186 ↗
• InjurySep 17, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT HAD INFECTION AND WAS WASHED OUT WITH POLY SWAP. UNKNOWN SURGICAL DELAY. DOI: UNKNOWN. DOR: (B)(6) 2024. AFFECTED SIDE: LEFT KNEE.

  Patient problems: Unspecified Infection

  MAUDE report 20238656 ↗
• InjuryFeb 8, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT'S KNEE WAS REVISED TO ADDRESS INSTABILITY. DOI: UNKNOWN, DOR: (B)(6) 2022, RIGHT KNEE.

  Patient problems: Joint Laxity

  MAUDE report 13481025 ↗
• InjuryFeb 1, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED TO ADDRESS INSTABILITY. SURGEON REMOVED THE 7X20 CRS POLY AND WENT UP TO A 26MM CRS POLY TO CORRECT PATIENT'S INSTABILITY. NO LOOSENING AND SURGICAL DELAY REPORTED. DOI: (B)(6) 2020, DOR: (B)(6) 2021, LEFT KNEE.

  Patient problems: Joint Laxity

  MAUDE report 11262970 ↗
• InjuryOct 6, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT WAS FELL AGAIN AND OPENED UP HER KNEE WOUND. SURGEON SWITCHED OUT THE POLY AGAIN AND THREW IN SOME ANTIBIOTICS BEADS TO HELP FIGHT OFF ANY INFECTION. DOI: (B)(6) 2020, DOR: (B)(6) 2020, LEFT KNEE.

  Patient problems: Fall; No Code Available; Unspecified Infection; Wound Dehiscence

  MAUDE report 10635901 ↗