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ATTUNE 1506-10-001Recalls & reported problems

Depuy (Ireland) · ATTUNE KNEE SYSTEM TIBIAL BASE ROTATING PLATFORM SIZE 1 CEMENTED · Class 3 · Implant

All models of ATTUNE (1475)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295042556), received between Jan 11, 2023 and Jan 11, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Migration” (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

Device problems

  • Migration1

Patient problems

  • Unspecified Tissue Injury1

Recent adverse event reports

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

  • InjuryJan 11, 2023Migration; Migration

    IT WAS REPORTED THAT ON (B)(6) 2019, THE PATIENT UNDERWENT THE SURGERY VIA TKA FOR LEFT OA WITH ATTUNE. THE SURGERY WAS COMPLETED SUCCESSFULLY WITHOUT ANY SURGICAL DELAY. AFTER THE SURGERY, PARTLY BECAUSE THE PATIENT'S BONES WERE FRAGILE, THE BONE INSIDE THE TIBIA GRADUALLY COLLAPSED, THE TIBIAL IMPLANT SUBSIDED, AND THE VARUS DEFORMITY BECAME STRONGER. THEREFORE, A REVISION SURGERY IS PLANNED ON (B)(6) 2023. NO FURTHER INFORMATION IS AVAILABLE.

    Patient problems: Unspecified Tissue Injury

    MAUDE report 16137079 ↗

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Sources and updates

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