DRIVEMEDICAL HCANE-BK-G2Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383571096), received between Mar 22, 2019 and Mar 22, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Material Twisted/Bent” (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 18, 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 22, 2019Material Twisted/Bent; Material Twisted/Bent

  (B)(4) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A CANE. THE CANE WAS DISCARDED BECAUSE IT WAS BROKEN. NO EXAMINATION AND ROOT CAUSE ANALYSIS CAN BE PERFORMED. THE CANE WAS PROVIDED TO THE END-USER IN AN ASSISTED LIVING FACILITY. HE FELL WHEN THE CANE BENT. IT IS BELIEVED THAT THE PUSH BUTTON MALFUNCTIONED. HE WAS HURT AND HOSPITALIZED. THE PATIENT BROKE HIS RIGHT HIP IN THE FALL. HE IS 6 FOOT 2 INCHES. HE REQUESTED A ROLLATOR INSTEAD OF A CANE REPLACEMENT BECAUSE HE BELIEVED THE CANE WAS UNSUITABLE FOR HIS AGE.

  Patient problems: Hip Fracture

  MAUDE report 8445261 ↗