Skip to content

Portable Suction Machine SU100DCRecalls & reported problems

Sunset Healthcare Solutions, Inc. · Portable Suction Machine · 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 00848530088965), received between Apr 6, 2023 and Apr 6, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Smoking” (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

  • Smoking1

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.

  • MalfunctionApr 6, 2023Smoking; Smoking

    THE PATIENT REPORTED ONE UNIT OF SU100DC THAT STARTED SMOKING WHILE USING THE UNIT. NO REPORT OF INJURY WAS RECEIVED. EVIDENCE SHOWS THAT THE UNIT BURNT OUT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16689225 ↗

Other Apparatus, Suction, Ward Use, Portable, Ac-Powered devices

All Apparatus, Suction, Ward Use, Portable, Ac-Powered devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.