Valkyrie® - Power Driver 01-03-3035Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08806390899796), received between Jan 29, 2026 and Jan 29, 2026 — 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 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.

• MalfunctionJan 29, 2026Electrical /Electronic Property Problem

  A CUSTOMER REPORTED THAT A VALKYRIE DISPOSABLE POWER DRIVER (REF. NO. (B)(4), LOT NO. 250021-1345, EXPIRATION DATE: 02/23/2028) MALFUNCTIONED DURING USE IN A CORONARY ARTERY BYPASS GRAFT (CABG) PROCEDURE. THE DEVICE DID NOT FUNCTION AS INTENDED WHILE BEING USED BY THE SURGEON. THE DRIVER WAS REMOVED FROM THE SURGICAL FIELD, AND A REPLACEMENT DEVICE WAS OPENED AND USED TO CONTINUE THE PROCEDURE. NO PATIENT INJURY WAS REPORTED.

  Patient problems: Unspecified Mental, Emotional or Behavioral Problem

  MAUDE report 24218420 ↗