Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 36882 |
| Brand Name: | Mindray BeneHeart C/D series AED - non rechargable |
| Model: | Mindray BeneHeart D1 AED |
| Affected: | Serial numbers - FQ-55068195, FQ-55068196, FQ-58068556, FQ-59068749, FQ-59068750 |
| Software version: | |
| Recalling Organisation: | Connected Healthcare Systems 6C Jack Conway Ave Manukau Auckland 2104 |
| Contact Information: | |
| Manufacturer: | Shenzhen Mindray Biomedical Electronics Co Ltd |
| Issue: | 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. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 11/6/2026 |
