ACCULAN 3TI GA672Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04038653404377), received between Mar 10, 2021 and Mar 10, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (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 16, 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.

• MalfunctionMar 10, 2021Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

  INVOLVED COMPONENT: GB638R - ACCULAN 3TI DRILL ATTACHM.LARGE JACOBS - 51926308 GB636R - ACCULAN 3TI DRILL ATTACHMENT HEXAG.CHUCK - 51872583 GA675 - ACCULAN LID ASSOCIATED MEDWATCH-REPORTS: 9610612-2021-00156(400503218 GA672) 9610612-2021-00160400503219 GB636R) 9610612-2021-00159(400503220 GB638R) 9610612-2021-00168(400503660 GA675).

  Patient problems: Insufficient Information

  MAUDE report 11455489 ↗