Mindray Beneheart C Series Aed
- Recalling firm
- Connected Healthcare Systems
- Product
- Mindray BeneHeart C series AED. [Device]. Model: BeneHeart C-Series Automated External Defibrillator
- Reason
- The operator's manual is being updated to help users better understand the impact of the Wi-Fi/cellular settings on battery life. Details of the modifications are as follows:, When the equipment is configured with the Wi-Fi/cellular module, it automatically sends self-test reports at preset intervals by default, which consumes battery power. Information has been updated in the manual to remind users that incorrect configuration of the wireless network would cause extra power consumption. Low battery power may cause the device to fail to power on, delaying therapy.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-02-20
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/14ece249-d1f1-4857-b226-c0f300cd26af