Hugo 700-979Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00754021210046), received between May 24, 2024 and May 27, 2024 — classified as 2 injuries.

The most frequently reported specific device problem is “Break” (2 reports).

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.

• InjuryMay 27, 2024Break; Break

  PER DRIVE DEVILBISS HEALTHCARE MDR #2438477-2024-00026: DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY THE END USER'S SON, WHO REPORTED THAT A PIN IN THE FRONT RIGHT LEG BROKE DURING USE CAUSING THE END USER TO FALL TO THE GROUND AND HIT HER HEAD. SHE RECEIVED A CT SCAN AND X-RAYS THAT REVEALED A LEFT BROKEN SHOULDER. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.

  Patient problems: Bone Fracture(s)

  MAUDE report 19400316 ↗
• InjuryMay 24, 2024Break; Break

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY THE END USER'S SON, WHO REPORTED THAT A PIN IN THE FRONT RIGHT LEG BROKE DURING USE CAUSING THE END USER TO FALL TO THE GROUND AND HIT HER HEAD. SHE RECEIVED A CT SCAN AND X-RAYS THAT REVEALED A LEFT BROKEN SHOULDER. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.

  Patient problems: Bone Fracture(s)

  MAUDE report 19397699 ↗