FDA Adverse Event Death Summary report: N

500 LB SMART LIFT WITH SCALE

MDR report key: 19714986 · Received July 10, 2024

Report

Report Number
2183887-2024-00003
Event Type
Death
Date Received
July 10, 2024
Date of Event
August 16, 2023
Report Date
June 28, 2024
Manufacturer
EZ WAY, INC
Product Code
FSA
UDI-DI
848914000057
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
NURSE
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

RESIDENT WAS IN ACTIVE DECLINE BEFORE THE INCIDENT OCCURED.

Description of Event or Problem · 0

2 CNAS WERE MOVING A RESIDENT FROM A TUB TO A WHEELCHAIR WITH A SLING AND SMART LIFT. THE CNAS HOOKED THE SLING UP TO THE HANGER BARS AND LIFTED THE RESIDENT. THE CNAS TURNED THE RESIDENT IN THE LIFT BY GUIDING THE LEGS. THE RESIDENT WAS MOVED 2-3 FEET TOWARDS THE WHEELCHAIR, AND ONE OF THE LOOPS BY THE LEGS CAME OFF THE HANGER BARS, AND THE RESIDENT FELL. THE RESIDENT HAD A LACERATION ON THE HEAD AND A FRACTURED HUMOROUS. THE RESIDENT WAS TAKEN TO THE ED (EMERGENCY DEPARTMENT) FOR STAPLES TO THE HEAD AND WAS TAKEN BACK TO THE HOSPICE DEPARTMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
352080 500 LB SMART LIFT WITH SCALE LIFT FSA EZ WAY, INC L500PS 848914000057

Patients

Seq Age Sex Outcome Treatment
1 NA Female Life Threatening| D