Hugo 731-850Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00754021210220), received between Mar 10, 2021 and Mar 10, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

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

• InjuryMar 10, 2021Material Fragmentation; Material Fragmentation

  DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A CANE. THE UNIT HAS NOT BEEN RETURNED FOR EVALUATION. WE WILL FILE A FOLLOW-UP SUBMISSION WHEN MORE DATA BECOMES AVAILABLE. WE ARE FILING THIRD REPORT IN AN OVER-ABUNDANCE OF CAUTION. WHILE IN USE ONE OF THE FOUR FEET BENT CAUSING THE END-USER TO FALL. HE RECEIVED CUTS ON HIS ARMS AND A PAIN IN HIS HIP. HE DID NOT GO TO THE HOSPITAL FOR TREATMENT. HE IS RECOVERING FROM HIP SURGERY.

  Patient problems: Fall; Laceration(s)

  MAUDE report 11456857 ↗