Precision Medical Inc. PM65HGRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00855887006597), received between Dec 9, 2016 and Dec 9, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Operational Issue” (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.

• MalfunctionDec 9, 2016Device Operational Issue; Device Operational Issue

  THESE ASPIRATORS BEHAVE AS IF THE BATTERY IS LOW/DISCHARGE WHEN TURNING THE UNIT ON. BIOMED TECH CALLED TECH SUPPORT AND ALSO LOOKED AT THE OPERATOR'S MANUAL WITH NO INDICATION OF THE ERROR WE WERE EXPERIENCING. AFTER OPENING THE UNIT, IT WAS NOTICED THAT THERE WAS A BLOWN FUSE. AFTER THE FUSE WAS REPLACED, THE UNIT STARTED TO WORK NORMAL AGAIN. SINCE THEN, WE HAVE IDENTIFIED AT LEAST 7 MORE DEVICES WITH THE SAME PROBLEM.

  Patient problems: No Patient Involvement

  MAUDE report 6159331 ↗