Precision Medical Inc. PM4150Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00855887006078), received between Sep 10, 2019 and Dec 31, 2019 — classified as 2 malfunctions.

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

• MalfunctionDec 31, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

  END USER CLAIMS PM4150 PORTABLE OXYGEN CONCENTRATOR CAUSED FIRE DAMAGE TO HOME UNKNOWN IF PRECISION MEDICAL PM4150 PORTABLE OXYGEN CONCENTRATOR GIVEN BY PATIENT WAS INVOLVED.

  Patient problems: No Code Available; No Known Impact Or Consequence To Patient

  MAUDE report 9536069 ↗
• MalfunctionSep 10, 2019Fire; Fire

  THE CLIENT THAT HAD THIS UNIT WAS MOWING HIS YARD; JUST LIKE HE HAD DONE MANY TIMES BEFORE WITH THE POC STRAPPED ONTO HIS BACK LIKE A BACKPACK. NOT SURE HOW; BUT HE SAID HE HAD LOOSENED THE STRAPS AND IT WAS RESTING ON THE BACK SEAT OF THE MOWER. IT MUST HAVE GOTTEN TOO CLOSE TO THE MUFFLER AS THAT IS WHAT THE CLIENT HAD STATED, AND IT BLEW UP & CAUGHT ON FIRE. IT SCARED THE CLIENT TO DEATH BUT HE WAS UNHARMED. FORTUNATELY, HE WAS CLOSE ENOUGH TO THE HOUSE THAT HE WAS ABLE TO GET INSIDE AND GET ON HIS CONCENTRATOR.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8983275 ↗