FDA Adverse Event Malfunction Summary report: N

DRIVE

MDR report key: 17088441 · Received June 8, 2023

Report

Report Number
2438477-2023-00061
Event Type
Malfunction
Date Received
June 8, 2023
Report Date
June 8, 2023
Manufacturer
COM-DA HEALTHCARE CO.,LTD
Product Code
IPS
UDI-DI
00754021210237
Product Problem
Yes
Report Source
Distributor report
Reporter Location
NV, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 0

DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF A COMPLAINT REGARDING A CANE BY AN END USER, WHO STATED THAT THE "[CANE] BASE IS NOT LARGE ENOUGH" AND THAT SHE FELL TO THE GROUND AND SUSTAINED BRUISING TO HER HIP WHILE USING IT, BUT DID NOT RECEIVE ANY MEDICAL TREATMENT. THE END USER SPECIFICALLY STATED THAT "THERE IS NOTHING WRONG WITH THE CANE EXCEPT SHE DOES NOT FEEL THE BASE IS BIG ENOUGH." DRIVE WILL CONTINUE TO MONITOR COMPLAINTS FOR ANY RELATED TRENDS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
270544 DRIVE CANE IPS COM-DA HEALTHCARE CO.,LTD 731-852 00754021210237

Patients

Seq Age Sex Outcome Treatment
1 75 YR Female