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Zimmer Biomet Patient Specific Instruments KNM-ZB02-00-01Recalls & reported problems

Materialise NV · ZB MRI TKA Biomet Pin Guide kit · Class 2

All models of Zimmer Biomet Patient Specific Instruments (2)

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

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.

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.

Recalls naming this device

  1. Apr 26, 2023Class IICompleted

    The wrong tibia guide was included intended for a different patient case.

    Z-2213-2023 · Root cause: Process control · Recall details · FDA record ↗

Other Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer devices

All Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer devices →

Sources and updates

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