FDA Adverse Event Injury Summary report: N

BED-CHECK

MDR report key: 507703 · Received January 15, 2004

Report

Report Number
507703
Event Type
Injury
Date Received
January 15, 2004
Date of Event
December 28, 2003
Report Date
December 30, 2003
Manufacturer
BED-CHECK CORP.
Product Code
KMI
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
TX, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PT FOUND ON FLOOR, PT FELL ON THEIR LEFT HIP WHICH WAS NOW HURTING. BEDCHECK WAS IN PLACE. BUT DID NOT ALARM AT TIME OF FALL. X-RAY SHOWED IMPACTED SUBCOPITAL LEFT FEMORAL NECK FRACTURE. PT HAD PROCEDURE TO REPAIR FRACTURE 12/2003.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BED-CHECK BED EXIT ALARM KMI BED-CHECK CORP. 100085-101 NA

Patients

Seq Age Sex Outcome Treatment
1 89 YR Required Intervention