Mindray Beneheart C/d Series Aed - Non Rechargable
- Recalling firm
- Connected Healthcare Systems
- Product
- Mindray BeneHeart C/D series AED - non rechargable. [Device]. Model: Mindray BeneHeart D1 AED. Affected: Serial numbers - FQ-55068195, FQ-55068196, FQ-58068556, FQ-59068749, FQ-59068750
- Reason
- To help users better understand the procedure for switching patient types on the Mindray BeneHeart D1 Automated External, Defibrillator (AED), the manufacturer has updated the Operator's Manual with refined guidance., When the device is set to paediatric mode and used for adult patients, there is a risk of ineffective defibrillation., This Operator's Manual revision only adds supplementary information. No changes have been made to the product itself or its, operational procedures.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-06-11
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/1889adf6-e60c-4f6e-bddd-19ae1ff42ec5