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Drive 13025Recalls & reported problems

Drive Devilbiss Healthcare · Patient RoomSlings Product Description: Sling,Polystr.for Lift 1/bx · Class 1

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 00822383103310), received between Feb 16, 2023 and Feb 16, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (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

  • Material Split, Cut or Torn1

Patient problems

  • Head Injury1

Recent adverse event reports

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

  • MalfunctionFeb 16, 2023Material Split, Cut or Torn; Material Split, Cut or Torn

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A PATIENT LIFT SLING BY AN END USER'S HUSBAND, WHO STATED THAT "THE SLING TORE, AND [HIS WIFE] FELL TO THE GROUND AND SUSTAINED A HEAD INJURY." THE END USER DID NOT SEEK ANY MEDICAL TREATMENT. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

    Patient problems: Head Injury

    MAUDE report 16388793 ↗

Other LIFT, PATIENT, NON-AC-POWERED devices

All LIFT, PATIENT, NON-AC-POWERED devices →

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