FDA Adverse Event Death Summary report: N

SLING USED W/LIFTER

MDR report key: 2101724 · Received May 18, 2011

Report

Report Number
2182305-2011-00014
Event Type
Death
Date Received
May 18, 2011
Date of Event
April 8, 2011
Report Date
April 22, 2011
Manufacturer
JOERNS HEALTHCARE
Product Code
FNG
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED TO MANUFACTURER, BY FACILITY; (B)(6), PER FACILITY, A ONE STAFF PERSON WAS MAKING THE LIFT TRANSFER, FROM THE SHOWER CHAIR TO THE RESIDENT BED, STAFF WAS HOLDING ONTO THE CORNER OF THE SLING AND TRYING TO GUIDE THE LIFT AT THE SAME TIME. WHILE TRYING TO RE-POSITION THE LIFT THE RESIDENT SLID OUT OF THE SLING AND FELL TO THE FLOOR AND HIT HER HEAD. RESIDENT WAS TAKEN TO HOSPITAL BY AMBULANCE ARRIVED AT THE HOSPITAL UNRESPONSIVE. CPR WAS INITIATED, HOWEVER RESIDENT DID NOT RESPOND. AT TIME OF INCIDENT, FACILITY WAS USING AN INCORRECT DEVICE COMBINATION I.E., A HOYER SLING MODEL 50020 ON THE TITAN X LIFT, (B)(6) RESIDENT IN A 600 LB SLING, WITH THE 1000 LB TITAN X LIFT. THE SLING MAY HAVE CONNECTED TO THE LIFT, BUT IT SOUNDS AS THOUGH THE EXTRA LARGE SLING WAS TOO BIG FOR THE RESIDENT, AND THE SLING AND LIFT ARE OF DIFFERENT MANUFACTURES. JOERNS, THE MANUFACTURER OF THE SLING, STATES IN OUR MANUALS AS WELL AS DIRECTLY APPLIED TO THE SLINGS "USE ONLY GENUINE HOYER PARTS; HOYER SLINGS AND LIFTERS ARE NOT INTERCHANGEABLE WITH OTHER MANUFACTURER'S PRODUCTS. USING OTHER MANUFACTURER'S PRODUCTS ON HOYER PRODUCTS IS UNSAFE AND MAY RESULT IN SERIOUS INJURY TO PT AND/OR CAREGIVER."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SLING USED W/LIFTER PATIENT SLING USED W/A PATIENT LIFTER FNG JOERNS HEALTHCARE 50020 SLING

Patients

Seq Age Sex Outcome Treatment
1 59 YR Death