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Drive 13263ERecalls & reported problems

Drive Devilbiss Healthcare · Sit-to-Stand-Sling-Med,1/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 00822383231723), received between Apr 21, 2023 and Apr 21, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Device Slipped” (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

  • Device Slipped1

Patient problems

  • Fall1
  • Head Injury1

Recent adverse event reports

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

  • InjuryApr 21, 2023Device Slipped; Device Slipped

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A SLING USED WITH A SIT-TO-STAND LIFT BY A PROVIDER, WHO STATED THAT "THE BELT ON SLING DOESN'T STAY TIGHT AND SLIDES LOOSE." THE END USER REPORTEDLY SLIPPED OUT OF THE SLING AND SUSTAINED A HEAD INJURY. THE END USER DID NOT SEEK ANY MEDICAL TREATMENT AS A RESULT OF THE INCIDENT. MULTIPLE ATTEMPTS TO GATHER FURTHER INFORMATION HAVE BEEN MADE, AND TO RETRIEVE THE PRODUCT FOR EVALUATION, BUT DRIVE HAS NOT RECEIVED A RESPONSE. DRIVE WILL CONTINUE TO MONITOR COMPLAINTS FOR ANY RELATED TRENDS.

    Patient problems: Fall; Head Injury

    MAUDE report 16787620 ↗

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.