FDA Adverse Event Injury Summary report: N

REHAND CANE

MDR report key: 22667132 · Received July 30, 2025

Report

Report Number
MW5173540
Event Type
Injury
Date Received
July 30, 2025
Date of Event
July 24, 2025
Report Date
July 24, 2025
Manufacturer
REHAND MEDICAL TECHNOLOGY CO., LTD.
Product Code
IPR
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
VA, US
Reporter Occupation
PATIENT
Health Professional
*

Narratives

Description of Event or Problem · 0

USING MY REHAND BRAND CANE THE HANDLE SUDDENLY SNAPPED OFF CAUSING ME TO FALL TO THE GROUND. THE PRODUCT WAS PURCHASED THROUGH AMAZON IN (B)(6) 2025. THE PART THAT GOES INTO THE METAL SHAFT IS JUST PLASTIC WITHOUT ANY METAL STIFFENING. LUCKILY, I WAS NOT USING STAIRS WHEN IT BROKE. IT IS RATED FOR 350 LBS AND I AM ABOUT 260 SO WELL WITHIN THE RATED USE. THERE WAS NO WARNING. CANE FOR MOBILITY HELP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
567923 REHAND CANE CRUTCH IPR REHAND MEDICAL TECHNOLOGY CO., LTD.

Patients

Seq Age Sex Outcome Treatment
1 73 YR Male Other