Precision Medical Inc. PM65Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00855887006580), received between Jul 25, 2022 and Jul 25, 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. 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.

• MalfunctionJul 25, 2022Fire; Fire

  CUSTOMER STATED WHEN STAFF CAME IN THE MORNING THEY SAW SOOT FROM AN APPARENT SMALL FIRE COVERING MOST OF THE EQUIPMENT ON THE INCUBATOR. THERE WAS NO FIRE WHEN THEY CAME IN THAT MORNING JUST THE BLACK SOOT. THE INCIDENT STATED HAPPENED OVERNIGHT WHEN NO ONE WAS AROUND. PRECISION MEDICAL INC PM65 ASPIRATOR WAS PART OF THE EQUIPMENT ON THE INCUBATOR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15095456 ↗