FDA Adverse Event Death Summary report: N

LIFT

MDR report key: 22923434 · Received August 29, 2025

Report

Report Number
2183887-2025-00005
Event Type
Death
Date Received
August 29, 2025
Report Date
August 29, 2025
Manufacturer
EZ WAY INC
Product Code
FSA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

EZ WAY RECEIVED THIS INFORMATION FROM A LAWYER REPRESENTING THE FAMILY.

Description of Event or Problem · 0

RESIDENT FELL OUT OF SLING. SLING WAS NOT HOOKED UP PROPERLY. RESIDENT SUSTAINED L5 AND L7 FRACTURE ALONG WITH A BAD HEAD BRUISE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2164244 LIFT FSA EZ WAY INC

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Death