FDA Adverse Event Malfunction Summary report: N

PRECISION FLOW

MDR report key: 2478479 · Received February 21, 2012

Report

Report Number
2478479
Event Type
Malfunction
Date Received
February 21, 2012
Date of Event
February 17, 2012
Report Date
February 21, 2012
Manufacturer
VAPOTHERM, INC
Product Code
BTT
Product Problem
Yes
Report Source
User Facility report
Reporter Location
CA, US

Narratives

Description of Event or Problem · 1

FLUID DID NOT FLOW, CAUSING UNIT TO BLOW DRY AIR TO PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PRECISION FLOW HUMIDIFIER BTT VAPOTHERM, INC PRECISION FLOW *

Patients

Seq Age Sex Outcome Treatment
1 *