FDA Adverse Event Malfunction Summary report: N

HOYER ADVANCE-E LIFT

MDR report key: 24414661 · Received February 23, 2026

Report

Report Number
3009402404-2026-00004
Event Type
Malfunction
Date Received
February 23, 2026
Date of Event
February 12, 2026
Report Date
February 23, 2026
Manufacturer
APEX HEALTH CARE MFG., INC
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
501

Narratives

Additional Manufacturer Narrative · 0

THIS REPORT OR OTHER INFORMATION SUBMITTED BY JOERNS HEALTHCARE UNDER 21 CFR PART 803, AND RELEASE BY FDA OF THAT REPORT INFORMATION, DOES NOT REFLECT A CONCLUSION OR ADMISSION BY JOERNS HEALTHCARE, ITS EMPLOYEES, ITS CONTRACT SERVICE FIRMS, OR THEIR EMPLOYEES, FINISHED DEVICE SUPPLIERS, OR THEIR EMPLOYEES CAUSED OR CONTRIBUTED TO THE REPORTABLE EVENT.

Description of Event or Problem · 0

IT WAS REPORTED TO THE MANUFACTURER BY THE END USER: THE PIN ASSEMBLY BELOW THE MOTOR UNIT ON OUR NEWER JOERNS LIFTS HAS FAILED X2. ONE FAILURE RESULTED IN A RESIDENT FALL WITH INJURY TO THE HEAD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
476021 HOYER ADVANCE-E LIFT PATIENT LIFT FSA APEX HEALTH CARE MFG., INC HOY-ADVANCE-E

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown