Proscope™ 5210Recalls & reported problems
American Diagnostic Corp · PROSCOPE Diagnostic Set,Standard, 2.5v · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00634782053413), received between May 20, 2022 and May 20, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fire” (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
Device problems
- Fire1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 20, 2022Fire; Fire
A CUSTOMER REPORTED THAT ADC'S PART NUMBER 5210, WHICH IS A 2.5V OTOSCOPE AND OPHTHALMOSCOPE, HAD ABNORMAL HEAT WHEN THEY ATTEMPTED TO USE IT AND THAT THE PRODUCT CAUGHT ON FIRE. NO INJURIES WERE REPORTED AND NO PATIENT INVOLVEMENT. THIS IS A HANDHELD, BATTERY OPERATED DEVICE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14462996 ↗
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.