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Catalyft PL Expandable Interbody System 6069113Recalls & reported problems

Medtronic Sofamor Danek, Inc. · SPACER 6069113 CATALYFT PL40 SHORT 11MM · Class 2 · Implant

All models of Catalyft PL Expandable Interbody System (16)

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. Sep 16, 2025Open, Classified

    Expandable interbody system cage may loose height or collapse (loss of lordosis), which could result in migration, subsidence and/or neurological injury. Therefore, surgical technique and instructions for use will be updated to mitigate risk of loss of lordosis to occur.

    Z-0580-2026 · Root cause: Labeling design · Recall details · FDA record ↗

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Sources and updates

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