FDA Adverse Event Death Summary report: N

BED RAIL

MDR report key: 29538 · Received December 26, 1995

Report

Report Number
MW4001029
Event Type
Death
Date Received
December 26, 1995
Date of Event
December 10, 1995
Report Date
December 22, 1995
Manufacturer
EVEREST & JENNINGS INTL., LTD.
Product Code
FNL
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
NY, US
Reporter Occupation
PHARMACIST

Narratives

Description of Event or Problem · 1

FAMILY REPORTED PT DIED FROM SUFFOCATION FROM GETTING BETWEEN HOSPITAL BED AND BED RAILS. CERTIFICATE OF DEATH SAID "CARDIORESPIRATORY ARREST DUE TO ALZHEIMER'S DEMENTIA." (ALSO SEE 4001036)

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BED RAIL BED RAIL FNL EVEREST & JENNINGS INTL., LTD. 149208

Patients

Seq Age Sex Outcome Treatment
1 74 YR Death