Category: Product correction · Supplier: Mindray Medical Australia Pty Ltd
Recall date:
Mindray Medical Australia Pty Ltd is conducting a product correction for the BeneHeart D1 Automated External Defibrillator. The operator’s manual is being updated for the procedure of switching patient types.
Mindray Medical Australia Pty Ltd is conducting a product correction for the BeneHeart D1 Automated External Defibrillator. The operator’s manual is being updated for the procedure of switching patient types.
Review the new electronic Operator’s Manual supplied by Mindray Medical Australia - BeneHeart D1 Automated External Defibrillator Operator’s Manual.As outlined in the manual, when the indicated patient type is different to the patient, you need to manually change the patient type.The Mindray BeneHeart D1 AED can be used as per routine practice.
Please contact Mindray Medical Australia on 1800 793 011 or email service.au@message.mindray.com for further information.
Explore more medicine recalls or run a broader search across all sources.