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Drive 18600-FILTERRecalls & reported problems

Drive Devilbiss Healthcare · Hydrophobic Filter ForSuctMachine,3/bx · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383151649), received between Sep 6, 2017 and Sep 6, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

  • Insufficient Device Problem Information1

Patient problems

  • Partial thickness (Second Degree) Burn1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjurySep 6, 2017Insufficient Device Problem Information

    DRIVE DEVILBISS HEALTHCARE RECEIVED A NOTIFICATION FROM AN ATTORNEY OF AN INCIDENT INVOLVING A SUCTION MACHINE THAT DRIVE IMPORTS AND DISTRIBUTES. THE PATIENT WAS SLEEPING WITH THE SUCTION MACHINE NEXT TO HIS BED WHEN ALLEGEDLY HE GOT BURNT. HE WAS TAKEN TO THE HOSPITAL WHERE IT WAS DISCOVERED HE HAD SUFFERED A 2ND DEGREE BURN FROM TOUCHING THE UNIT.

    Patient problems: Partial thickness (Second Degree) Burn

    MAUDE report 6847027 ↗

Other TUBING, PRESSURE AND ACCESSORIES devices

All TUBING, PRESSURE AND ACCESSORIES devices →

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