FDA Adverse Event Injury Summary report: N

EZ WAY SMART LIFT

MDR report key: 17240080 · Received June 29, 2023

Report

Report Number
MW5119032
Event Type
Injury
Date Received
June 29, 2023
Date of Event
June 20, 2023
Report Date
June 27, 2023
Manufacturer
EZ WAY, INC.
Product Code
FSA
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
IA, US
Reporter Occupation
501
Health Professional
Yes

Narratives

Description of Event or Problem · 0

EZ WAY SMART LIFT RATED FOR 500 LBS. FAILED WHEN THE ACTUATOR GAVE OUT WHILE THE LIFT WAS ENGAGED TO LIFT THE RESIDENT. RESIDENT FELL TO THE FLOOR, FALLING APPROXIMATELY 4 FEET. NO MAJOR INJURY DETERMINED FROM THE FALL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1207764 EZ WAY SMART LIFT LIFT, PATIENT, NON-AC-POWERED FSA EZ WAY, INC. L500PS

Patients

Seq Age Sex Outcome Treatment
1 70 YR Male Required Intervention