Dental Putty Cartridge 4 x 0.5cc NA3640Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00813909010755), received between Jan 16, 2017 and Jan 16, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Device Operates Differently Than Expected” (1 report).

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.

Most reported problems

Recent adverse event reports

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

• InjuryJan 16, 2017Device Operates Differently Than Expected

  APPROXIMATELY 6 FAILURES OF DENTAL PUTTY TO REMODEL IN PATIENTS WITH ABSCESSED TEETH. THE "MUSHY MATERIAL" (BELIEVED TO BE NOVABONE PUTTY) WAS REMOVED AND THE AREA RE-GRAFTED BY THE SURGEON. NO FINAL OUTCOME IS KNOW AT THIS POINT.

  Patient problems: Failure of Implant

  MAUDE report 6254566 ↗