FDA Adverse Event Death Summary report: N

LAERDAL SUCTION UNIT (LSU)

MDR report key: 619957 · Received July 8, 2005

Report

Report Number
9610483-2005-00022
Event Type
Death
Date Received
July 8, 2005
Date of Event
November 14, 2004
Report Date
December 2, 2004
Manufacturer
ASMUND S. LAERDAL A/S
Product Code
BTA
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
EMERGENCY MEDICAL TECHNICIAN

Narratives

Description of Event or Problem · 1

DURING AN INCIDENT IN 04 INVOLVING A PATIENT, THE SUCTION UNIT FAILED TO SUCTION THE PATIENT'S VOMIT. THE INCIDENT DESCIPTION READ: "PATIENT SUSPENDED VF - SHOCKED + PT VOMITED, ATTEMPTED TO SUCTION PATIENT, SUCTION COMPETELY EFFECTIVE. 2ND CREW ARRIVED - THEIR OLD TYPE LSU ALSO USELESS, THEREFORE UNABLE TO SECURE AIRWAY, " THE PATIENT DIED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LAERDAL SUCTION UNIT (LSU) PORTABLE SUCTION UNIT BTA ASMUND S. LAERDAL A/S * *

Patients

Seq Age Sex Outcome Treatment
1 37 YR Death