ATTUNE 1517-10-314Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295055723), received between Jan 2, 2020 and Jan 2, 2020 — classified as 1 injury.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJan 2, 2020Unintended Movement; Unintended Movement

  THE PRIMARY SURGERY WAS PERFORMED ON (B)(6) 2019 VIA TKA WITH THE INSERT (P/N: 151710314). AFTER THE PRIMARY SURGERY, THE PATIENT REPORTED THAT WHEN SHE BENT HER KNEES, THERE WAS INSTABILITY. IT WAS REPORTED THAT ON (B)(6) 2019, THE INSERT WAS REPLACED WITH AN UNKNOWN INSERT (20 MM) IN THE REVISION SURGERY. BEFORE THE REVISION SURGERY, THE SURGEON CHECKED THE INFECTION, AND THE RESULT WAS NEGATIVE. DURING THE SURGERY, THE SURGEON MADE AN INCISION, AND HE FOUND THAT THE INSERT SPUN-OUT. THE SURGEON WASHED OUT AND REPLACED THE INSERT WITH AN UNKNOWN INSERT (20 MM). THE SURGERY WAS COMPLETED SUCCESSFULLY. THE SURGICAL DELAY IS UNKNOWN. NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Code Available

  MAUDE report 9539946 ↗