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TSI DS-0014Recalls & reported problems

Tedan Surgical Innovations, L.L.C. · DISTRACTION SCREW, 14 MM, STERILE, 5/BOX · Class 1

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

Recalls naming this device

  1. May 15, 2020Terminated

    Lack of pouch seal. Product is labelled as sterile.

    Z-2527-2020 · Root cause: Packaging change control · FDA record ↗

Other Orthopedic Manual Surgical Instrument devices

All Orthopedic Manual Surgical Instrument devices →

Sources and updates

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