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nanOss 3D Advanced Bone Graft Substitute 90-300-25508Recalls & reported problems

Xtant Medical Holdings, Inc. · Advanced Bone Graft Substitute 10cc · Class 2 · Implant

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 9, 2026Open, Classified

    Products were incorrectly labeled with a 5-year shelf life. The approved and validated shelf life is four years.

    Z-1897-2026 · Root cause: Incorrect or no expiration date · FDA record ↗

Other Filler, Bone Void, Calcium Compound devices

All Filler, Bone Void, Calcium Compound devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.