Drive HCANE-PR-C2Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383575964), received between Dec 17, 2019 and Dec 17, 2019 — 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. How this data works · Data updated Oct 13, 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.

• InjuryDec 17, 2019Material Fragmentation; Material Fragmentation

  DRIVE DEVILBISS IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A HURRYCANE BRANDED CANE. WE HAVE NOT RECEIVED THE DEVICE FOR EVALUATION. AN AMENDED REPORT WILL BE TENDERED IF THE DEVICE IS RETURNED. END-USER WAS CARRYING TRASH WHILE USING THE CANE. THE HANDLE BROKE OFF FROM THE DEVICE. THE END-USER FELL BACKWARDS HITTING THE LEFT SIDE OF HIS FACE ON THE SIDEWALK. HE BLED FROM HIS LEFT EYEBROW. HE WAS CONFUSED AND DISORIENTED. HE WENT TO THE HOSPITAL TO TREAT HIS INJURIES. X-RAYS REVEALED A STABLE BREAK OF HIS WRIST. HE RECEIVED STITCHES FOR HIS EYEBROW AND PAIN MEDICATIONS FOR HIS INJURIES. HE UNDERWENT PHYSICAL THERAPY FOR HIS NECK AND WRIST PAIN.

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

  MAUDE report 9484621 ↗