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ATTUNE 1517-30-522Recalls & reported problems

Depuy (Ireland) · ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 22mm P · Class 2 · Implant

All models of ATTUNE (1475)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

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

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

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 16, 2026.

Recalls naming this device

  1. May 19, 2026Open, Classified

    The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

    Z-2617-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Other PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER devices

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Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page