Beneheart C Series Aed: Non-rechargeable Public Automated External Defibrillator
BeneHeart C Series AED Recall Summary Mindray Medical Australia is correcting BeneHeart C Series Automated External Defibrillators (AEDs) that are distributed across Australia. The specific reason for the correction has not been detailed in the available information. This is classified as a Class I correction, which indicates a serious issue affecting the device's safety or effectiveness.
- Reason
- Mindray Medical Australia Pty Ltd is conducting a product correction for the BeneHeart C Series Automated External Defibrillator (AED).
- Classification
- Class I
- Category
- medical device recall
- Country
- Australia
- Agency
- Therapeutic Goods Administration
- Recall date
- 2026-01-29
- Status
- Ongoing
- Distribution
- Australia-wide
Official recall notice from Therapeutic Goods Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/dbece038-a389-40a7-9afe-adda195e704a