Tapered Screw-Vent® Implant System ACTTRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024013704), received between Jul 27, 2022 and Jul 27, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unintended Movement” (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.

• MalfunctionJul 27, 2022Unintended Movement; Unintended Movement

  IT WAS REPORTED THAT THE ABUTMENT SCREW LOOSENED AT THE SITE. THE PATIENT REFLECTED THAT HE FELT UNWELL WHEN EATING AND DID NOT KNOW IF IT WAS CAUSED BY THE SCREW LOSS. THE RESTORATION WAS REMOVED. PAIN WAS ALSO REPORTED.

  Patient problems: Pain

  MAUDE report 15113514 ↗