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Stablecut® 19075127YT1Recalls & reported problems

Zimmer Orthopaedic Surgical Products, Inc. · Class 1

All models of Stablecut (11)

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. Jul 27, 2018Class IITerminated

    Mislabeled: Actual blade width is 19 mm but the label indicates a width of 25 mm.

    Z-1676-2020 · Root cause: Labeling Change Control · Recall details · FDA record ↗

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Sources and updates

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