Skip to content

MacroPor-Si+ 10.0 cc NB2510Recalls & reported problems

Novabone Products, LLC · Synthetic bone void filler for orthopedic applications · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00813909011066), received between Jan 16, 2017 and Jan 16, 2017 — classified as 1 injury.

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.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Unspecified Infection1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJan 16, 2017Adverse Event Without Identified Device or Use Problem

    DR. (B)(6) REPORTED THREE INFECTIONS IN RECENT SURGERIES. THE PHYSICIAN RAN CULTURES ON THE THREE IMPLANT GRAFTS PRIOR TO IMPLANTATION. ALL CULTURE RESULTS WERE NEGATIVE FOR ALL THREE CULTURES.

    Patient problems: Unspecified Infection

    MAUDE report 6254575 ↗

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.