FDA Adverse Event Death Summary report: N

LSP EMERGENCY VENTILATOR

MDR report key: 292117 · Received August 18, 2000

Report

Report Number
1924066-2000-00006
Event Type
Death
Date Received
August 18, 2000
Report Date
August 17, 2000
Manufacturer
ALLIED HEALTHCARE PRODUCTS, INC.
Product Code
BTL
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NM, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

PATIENT VALVE NOT FUNCTIONING, PT EXPIRED. PT VALVE APPEARED TO HAVE BEEN DROPPED AS PT VALVE HOUSING WAS CRACKED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LSP EMERGENCY VENTILATOR EMERGENCY VENTILATOR BTL ALLIED HEALTHCARE PRODUCTS, INC. L460 NA

Patients

Seq Age Sex Outcome Treatment
1 * Death