DRIVEMEDICAL HCANE-ROLL-RDRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383584775), received between Sep 19, 2019 and Sep 19, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Device Slipped” (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.

• InjurySep 19, 2019Device Slipped; Device Slipped

  DRIVE DEVILBISS IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A ROLLATOR. WE ARE STILL AWAITING RETURN OF THE DEVICE FOR EVALUATION. WE WILL FILE A FOLLOWUP AFTER EVALUATION HAS OCCURED. THE END-USER WAS DESCENDING THE STAIRS WHEN THE DEVICE "SHIFTED." THE USER FELL. SHE HIT THE LEFT SIDE OF HER FACE AND HER LEFT KNEE. THE LEFT KNEE HAD UNDERGONE A KNEE REPLACEMENT IN THE PAST. UPON INVESTIGATION IT WAS NOTED THAT A SCREW HAD COME OUT OF THE DEVICE. THIS SCREW HAD REPORTEDLY CAME OUT OF THE DEVICE ON A PRIOR OCCASION.

  Patient problems: Bruise/Contusion; Fall

  MAUDE report 9090240 ↗