Beneheart D1 Aed: Non-rechargeable Public Automated External Defibrillator
Mindray Medical Australia is correcting the operator's manual for the BeneHeart D1 Automated External Defibrillator, which is used to treat cardiac emergencies in public settings. The manual instructions for switching between patient types are being updated. This correction affects BeneHeart D1 devices distributed throughout Australia.
- Reason
- 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.
- Classification
- Class I
- Category
- medical device recall
- Country
- Australia
- Agency
- Therapeutic Goods Administration
- Recall date
- 2026-06-02
- Status
- Ongoing
- Distribution
- Australia-wide
Official recall notice from Therapeutic Goods Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/056faf99-b583-41a7-ba57-a4be2423ecb1