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Hugo 700-961Recalls & reported problems

Drive Devilbiss Healthcare · Rollators4-Wheel Alum Product Description: Hugo Elite Roll KD, Red, 1EA, 2CV, Ret. · 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 00754021210893), received between Nov 25, 2020 and Nov 25, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Solder Joint Fracture” (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

  • Solder Joint Fracture1

Patient problems

  • Fall1

Recent adverse event reports

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

  • InjuryNov 25, 2020Solder Joint Fracture; Solder Joint Fracture

    DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE, WHICH IS A ROLLATOR. THE DEVICE HAS NOT BEEN RECOVERED FOR EVALUATION. A FOLLOW-UP REPORT WILL BE SUBMITTED, ONCE THERE IS ADDITIONAL INFORMATION AVAILABLE. WHILE IN USE THE FORK ASSEMBLY DETACHED FROM THE FRAME. THE USER FELL, AND HIT HER HEAD.

    Patient problems: Fall

    MAUDE report 10906339 ↗

Other WALKER, MECHANICAL devices

All WALKER, MECHANICAL devices →

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