HOPKINS 7220BARecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048551193372), received between Mar 7, 2026 and Mar 7, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Display or Visual Feedback 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 7, 2026Display or Visual Feedback Problem

  THE FOLLOWING WAS REPORTED: "THE SCOPE WAS CONNECTED TO THE TOWER, AND HE WAS NOT ABLE TO EXAMINE THE PATIENT USING THE SCOPE. THERE WAS NO IMAGE SHOWING ON THE SCREEN; THE SCREEN WAS BLACK. THERE IS NO PHYSICAL DAMAGE ON THE SCOPE. THE SCOPE WAS CONNECTED ON A DIFFERENT TOWER AND THERE WAS NO IMAGE SHOWING ON THE SCREEN AGAIN." NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24540745 ↗