ATTUNE 1506-70-001Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295492030), received between Oct 23, 2020 and Oct 23, 2020 — classified as 1 injury.

1 other recall cover devices cleared under the same FDA submission (K170806, K233980); they may or may not involve this specific model.

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.

• InjuryOct 23, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED TO ADDRESS PAIN AND INSTABILITY. TIBIAL REVISION WAS PERFORMED. INFORMATION ON RETAINED COMPONENTS WAS NOT AVAILABLE. NO SURGICAL DELAY. DOI: UNKNOWN; DOR: (B)(6) 2020; RIGHT KNEE.

  Patient problems: No Code Available; Pain

  MAUDE report 10726494 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K170806, K233980. One submission often covers many models, so check the product and lot details in each record.

• Z-1314-2021 · Feb 22, 2021 · Terminated
  ATTUNE FIXED BEARING KNEE - Product Usage: composed of individually packaged femoral, tibial and patellar components designed to replace the natural articular surface of the knee