FDA Adverse Event Other Summary report: N

AIRLIFE

MDR report key: 18239925 · Received November 29, 2023

Report

Report Number
MW5148602
Event Type
Other
Date Received
November 29, 2023
Report Date
November 27, 2023
Manufacturer
VYAIRE MEDICAL INC.
Product Code
BTT
Report Source
Voluntary report
Reporter Occupation
PHARMACIST
Health Professional
Yes

Narratives

Description of Event or Problem · 0

WRONG SOLUTION CONNECTED TO THE HEATER OF A VENTILATOR GIVEN LOOK-ALIKE RISK OF VYAIRE SOLUTION BAG WITH BAXTER D5W 0.45% NS L BAGS. MESSAGED VYAIRE TO URGE CHANGING THE COLOR OF THE WORD 'INHALATION' OR ANOTHER VISUAL IDENTIFIER ON THE BAG? THANK YOU!

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1430420 AIRLIFE HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE) BTT VYAIRE MEDICAL INC. Q2211210

Patients

Seq Age Sex Outcome Treatment
1 Unknown BAXTER D5W 0.45% NS.