DRIVEMEDICAL 146-10301F-4Recalls & reported problems
Drive Devilbiss Healthcare · Canes & CrutchesQuad Canes Product Description: Quad Cane,Sm.Base,FoamGrp,Chrm,4/cs · Class 1
All models of DRIVEMEDICAL (111)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00612479222694), received between Sep 25, 2024 and Mar 20, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break1
- Insufficient Device Problem Information1
Patient problems
- Bruise/Contusion1
- Laceration(s)1
- Limb Fracture1
- Vertigo1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 20, 2025Break; Break
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A QUAD CANE BY A PROVIDER WHO REPORTED THAT THE CANE BROKE WHILE IN USE CAUSING THE END-USER TO FALL TO THE GROUND AND FRACTURE THEIR SHOULDER. THE DEVICE WAS RETURNED FOR EVALUATION. UPON EVALUATION, IT WAS OBSERVED THAT THE CANE SHAFT TUBE WAS BROKEN BY THE DETENT BUTTONHOLE. THERE WERE NO OTHER VISIBLE DEFECTS IDENTIFIED TO THE DEVICE THAT MAY HAVE LED TO THE REPORTED MALFUNCTION. THE MANUFACTURER WILL ALSO BE NOTIFIED OF THIS INCIDENT.
Patient problems: Limb Fracture
MAUDE report 21653765 ↗InjurySep 25, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A CANE BY THE END USER WHO STATED THE CANE COLLAPSED WHILE IN USE CAUSING THE END USER TO FALL. THE END USER REPORTED SUSTAINING MULTIPLE INJURIES, INCLUDING VERTIGO AND "BLACKING OUT," UNSPECIFIED INJURY TO HIS RIGHT KNEE, AND CUTS AND BRUISES TO HIS EYE AND ARM, RESULTING IN A THREE-DAY HOSPITALIZATION AND SUBSEQUENT FALLS CAUSING FURTHER INJURY TO HIS RIBS AND SPINE. 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: Bruise/Contusion; Laceration(s); Vertigo
MAUDE report 20301609 ↗
Other CANE devices
- DRIVEMEDICAL HCANE-BK-C2Drive Devilbiss Healthcare · CANE6 reports
- Hugo 731-852Drive Devilbiss Healthcare · CANE2 reports
- DRIVEMEDICAL HCANE-BL-C2Drive Devilbiss Healthcare · CANE2 reports
- Drive HCANE-PR-C2Drive Devilbiss Healthcare · CANE1 report
- Drive RTL10372BKDrive Devilbiss Healthcare · CANE1 report
- DRIVEMEDICAL HCANE-BK-G2Drive Devilbiss Healthcare · CANE1 report
- HUGO 731-840Drive Devilbiss Healthcare · CANE1 report
- Hugo 731-850Drive Devilbiss Healthcare · CANE1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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