HOPKINS 7220AARecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04048551193365), received between Jun 18, 2025 and Oct 29, 2025 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryOct 29, 2025Overheating of Device; Overheating of Device

  IT WAS REPORTED "ENT SURGEON COMPLAINED OF A BURNED FINGER FROM USING THE 0-DEGREE SCOPE. SINCE THE DESCRIPTION INDICATES THAT THE SURGEON BURNED A FINGER, THE EVENT IS DEEMED REPORTABLE.

  Patient problems: Burn(s)

  MAUDE report 23414650 ↗
• MalfunctionJun 18, 2025Break; Optical Problem; Break; Optical Problem

  IT HAS BEEN REPORTED THE SCOPE WAS BENT AND BLURRY. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22284857 ↗