FDA Adverse Event Death Summary report: N

VENTLAB AMBU BAG

MDR report key: 363227 · Received November 28, 2001

Report

Report Number
363227
Event Type
Death
Date Received
November 28, 2001
Date of Event
November 26, 2001
Report Date
November 27, 2001
Manufacturer
VENTLAB CORPORATION
Product Code
BTM
Product Problem
Yes
Report Source
User Facility report
Reporter Location
MO, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PT WENT INTO CARDIAC ARREST. CRASH CART BROUGHT TO ROOM. DISPOSABLE AMBU BAG WOULDN'T INFLATE; HAD TO OBTAIN REPLACEMENT (TOOK APPROX ONE-TWO MINUTES). CODE CARRIED OUT BUT PT EXPIRED. UNSURE IF ONE-TWO MINUTES DELAY IMPACTED OUTCOME OR NOT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
53566 VENTLAB AMBU BAG DISPOSABLE AMBU BAG BTM VENTLAB CORPORATION VN 1000 SERIES UNK

Patients

Seq Age Sex Outcome Treatment
1 79 YR Death