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DURAFORM 80-1477USRecalls & reported problems

Cerenovus, Inc. · DURAFORM Dural Graft Implant 3 Inches x 3 Inches (7.62cm x 7.62cm) · Class 2 · Implant

All models of DURAFORM (4)

Data updated Oct 18, 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 18, 2026.

Recalls naming this device

  1. Sep 26, 2024Class IIOpen, Classified

    Out of specification endotoxin levels.

    Z-0262-2025 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗

Other DURA SUBSTITUTE devices

All DURA SUBSTITUTE devices →

Sources and updates

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