FDA Adverse Event Injury Summary report: N

JOERNS MANUAL HI-LOW BED & FULL LENGTH SIDE RAIL

MDR report key: 35435 · Received July 1, 1996

Report

Report Number
35435
Event Type
Injury
Date Received
July 1, 1996
Date of Event
February 6, 1996
Report Date
February 15, 1996
Manufacturer
SUNRISE MEDICAL JOERNS
Product Code
FNJ
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE RESIDENT IN QUESTION IS A SMALL MAN WITH A DIAGNOSIS OF DEMENTIA AND CVA. THIS INCIDENT OCCURRED WHILE HE WAS IN BED. HE HAD BEEN CHECKED BY THE NURSE AT 2:00 AM AND WAS IN THE CENTER OF THE BED. AT 2:35 AM HE WAS FOUND LODGED BETWEEN THE BED RAIL AND THE BED FRAME. HE HAD TURNED AND SCOOTED HIMSELF AND PUSHED UNTIL ABOUT HALF OF HIS BODY WAS BETWEEN THE BED RAIL AND BED FRAME. WHEN HE WAS FOUND HE WAS UNRESPONSIVE, COLD AND MOTTLED SOME. HE WAS MANUALLY REMOVED, OXYGEN WAS STARTED AND HE DID RESPOND QUICKLY. HE SEEMS TO BE FINE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 JOERNS MANUAL HI-LOW BED & FULL LENGTH SIDE RAIL MANUAL HI-LOW BED & FULL LENGTH SIDE RAIL FNJ SUNRISE MEDICAL JOERNS 1005, 180 UNK

Patients

Seq Age Sex Outcome Treatment
1 75 YR Life Threatening| R