HUGO 731-840Recalls & reported problems
Drive Devilbiss Healthcare · HUGO LARGE QUAD, EBONY, 1EA, 2CV, RET. · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07540212101902), received between Sep 19, 2022 and Sep 19, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Integrity Problem” (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
- Material Integrity Problem1
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.
MalfunctionSep 19, 2022Material Integrity Problem; Material Integrity Problem
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A CANE BY AN END USER, WHO REPORTED THAT WHO REPORTED THAT THE CANE COLLAPSED, CAUSING HIM TO FALL AND HURT HIS SHOULDER AND REQUIRED PHYSICAL THERAPY TREATMENTS. DRIVE DID NOT GET THE PRODUCT BACK FOR EVALUATION.
Patient problems: Fall
MAUDE report 15447683 ↗
Other CANE devices
- DRIVEMEDICAL HCANE-BK-C2Drive Devilbiss Healthcare · CANE6 reports
- DRIVEMEDICAL 146-10301F-4Drive Devilbiss Healthcare · CANE2 reports
- Hugo 731-852Drive Devilbiss Healthcare · CANE2 reports
- DRIVEMEDICAL HCANE-BL-C2Drive Devilbiss Healthcare · CANE2 reports
- Drive RTL10310Drive Devilbiss Healthcare · CANE1 report
- Drive RTL10342Drive Devilbiss Healthcare · CANE1 report
- Hugo 731-850Drive Devilbiss Healthcare · CANE1 report
- DRIVEMEDICAL HCANE-BK-G2Drive Devilbiss Healthcare · CANE1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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