TRUMPF MEDICAL 1489491Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887761993075), received between Mar 24, 2022 and Mar 24, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (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.

• MalfunctionMar 24, 2022Loss of or Failure to Bond; Loss of or Failure to Bond

  THE CUSTOMER REPORTED, THE SHUTTLE WAS RAISED (HEIGHT ADJUSTMENT UP) WHEN THE GUIDING TUBE (WHICH COVERS THE HYDRAULIC CYLINDER OF THE HEIGHT ADJUSTMENT) CAME OUT OF THE BASE. IN THIS CONDITION THE SHUTTLE IS NO LONGER STABLE. NO PATIENT WAS INVOLVED IN THE EVENT AND NO INJURY WAS REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13882054 ↗