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HUGO 700-957 (UDI 07540212100226)Recalls & reported problems

Drive Devilbiss Healthcare · HUGO OPP PACIFIC BLUE, 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 07540212100226), received between Sep 13, 2022 and Sep 13, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Defective Component” (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

  • Defective Component1

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.

  • InjurySep 13, 2022Defective Component; Defective Component

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED BY AN END USER OF AN INCIDENT INVOLVING A ROLLATOR. THE END USER REPORTED THAT "THE ARMS ARE NOT SECURED TO MY CHAIR," AND THAT "ONE OF THE RUBBER ARMS CAME OFF AND I BROKE MY COLLAR BONE." THE END USER REPORTED GOING TO THE EMERGENCY ROOM. THE END USER REPORTED THAT HE WAS "NOT ABLE TO RETURN THE UNIT" FOR EVALUATION. DRIVE WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

    Patient problems: Fall

    MAUDE report 15411990 ↗

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.