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Drive 10244-4Recalls & reported problems

Drive Devilbiss Healthcare · Walker,Steel, Adult 2Button 5inWhls,4/CS · Class 1

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 50822383515620), received between Jun 4, 2020 and May 7, 2026 — classified as 2 injuries.

The most frequently reported specific device problem is “Material Twisted/Bent” (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 16, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 1 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Material Twisted/Bent1
  • Use of Device Problem1

Patient problems

  • Bone Fracture(s)1
  • Fall1
  • Laceration(s)1

Recent adverse event reports

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

  • InjuryMay 7, 2026Use of Device Problem

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WALKER BY THE END USER, WHO REPORTED THAT WHILE USING THE WALKER, THE WALKER HIT A CRACK AND STOPPED ABRUPTLY, CAUSING HER TO FALL OVER THE TOP OF THE WALKER AND SUSTAIN A FRACTURE IN THE TIP OF HER TIBIA. THERE WAS NO SPECIFIED DEFECT IN OR MALFUNCTION OF THE DEVICE. PRODUCT LABELING STATES,"BE AWARE OF THE FOLLOWING, GAPS IN THE FLOOR." AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.

    Patient problems: Bone Fracture(s)

    MAUDE report 25110559 ↗
  • InjuryJun 4, 2020Material Twisted/Bent; Material Twisted/Bent

    DRIVE DEILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WALKER. WE HAVE RECEIVED PHOTOS OF THE DAMAGED DEVICE. END-USER IS NOT RETURNING THE DEVICE FOR EVALUATION. SPOUSE REPORTED THAT WALKER DISPENSED TO PATIENT FAILED AS ONE OF THE LEGS ON THE WALKER BENT;. PATIENT FELL HITTING HIS HEAD RESULTING IN BLEEDING THE FOLLOWING DATA IS FROM NOTES FROM PHYSICAL THERAPY ASSOCIATE WITH ASSESSMENT INITIAL VISIT ON WHEN WALKER RECEIVED. PATIENT IS HOMEBOUND WITH POOR ENDURANCE AND SOB WITH MINIMAL ACTIVITY, GAIT IS LIMITED TO HOUSEHOLD DISTANCES. PATIENT IDENTIFIED AS HIGH RISK TO FALL ENVIRONMENT DESCRIBED AS CLUTTERED, PETS POORLY CONTROLLED, SLIP HAZARDS PRESENT. PATIENT VERY UNSAFE WITH ROLLING WALKER.

    Patient problems: Fall; Laceration(s)

    MAUDE report 10119546 ↗

Other WALKER, MECHANICAL devices

All WALKER, MECHANICAL devices →

Sources and updates

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