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Hugo 700-959 (UDI 07540212108864)Recalls & reported problems

Drive Devilbiss Healthcare · Hugo Elite Roll KD, 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 07540212108864), received between Sep 6, 2022 and Sep 6, 2022 — classified as 1 injury.

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

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

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

Recent adverse event reports

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

  • InjurySep 6, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    DRIVE DEVILBISS HEALTHCARE RECEIVED A COMPLAINT INVOLVING A ROLLATOR FROM AN END USER, WHO REPORTED THAT A "BRAKE FAILURE CAUSED HER TO FALL AND SUSTAIN INJURY." THE END USER SOUGHT MEDICAL TREATMENT FOR A WOUND ON HER LEG, AS WELL AS A "FRACTURED LUMBAR." DRIVE PROVIDED A REPLACEMENT MODEL TO THE END USER, AND IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT TO EVALUATE IT.

    Patient problems: Bone Fracture(s); Laceration(s)

    MAUDE report 15364233 ↗

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.