Hugo 731-852Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00754021210237), received between Jun 8, 2023 and Jul 5, 2023 — classified as 2 malfunctions.

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

Recent adverse event reports

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

• MalfunctionJul 5, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF A COMPLAINT REGARDING A CANE BY AN END USER, WHO STATED THAT THE "[CANE] BASE IS NOT LARGE ENOUGH" AND THAT SHE FELL TO THE GROUND AND SUSTAINED BRUISING TO HER HIP WHILE USING IT, BUT DID NOT RECEIVE ANY MEDICAL TREATMENT. THE END USER SPECIFICALLY STATED THAT "THERE IS NOTHING WRONG WITH THE CANE EXCEPT SHE DOES NOT FEEL THE BASE IS BIG ENOUGH." DRIVE WILL CONTINUE TO MONITOR COMPLAINTS FOR ANY RELATED TRENDS.

  Patient problems: Fall

  MAUDE report 17255541 ↗
• MalfunctionJun 8, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF A COMPLAINT REGARDING A CANE BY AN END USER, WHO STATED THAT THE "[CANE] BASE IS NOT LARGE ENOUGH" AND THAT SHE FELL TO THE GROUND AND SUSTAINED BRUISING TO HER HIP WHILE USING IT, BUT DID NOT RECEIVE ANY MEDICAL TREATMENT. THE END USER SPECIFICALLY STATED THAT "THERE IS NOTHING WRONG WITH THE CANE EXCEPT SHE DOES NOT FEEL THE BASE IS BIG ENOUGH." DRIVE WILL CONTINUE TO MONITOR COMPLAINTS FOR ANY RELATED TRENDS.

  Patient problems: Fall

  MAUDE report 17088441 ↗