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SMART TOE ST0XS-11Recalls & reported problems

Stryker GmbH · Intramedullary Arthrodesis Implant · Class 2 · Implant

Data updated Oct 13, 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Mar 28, 2022Open, Classified

    The nickel-sensitivity statement on the outer carton may be partially covered by a label resulting in the statement showing "Indicated for patients with Nickel sensitivity" instead of "Not Indicated for patients with Nickel sensitivity".

    Z-1011-2022 · Root cause: Process control · FDA record ↗

Other PIN, FIXATION, SMOOTH devices

All PIN, FIXATION, SMOOTH devices →

Sources and updates

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