Beneheart D30/60/dx Aed/manual Defibrillator/monitor
- Recalling firm
- Connected Healthcare Systems
- Product
- Beneheart D30/60/DX AED/Manual Defibrillator/Monitor. [Device]. Model: Multiple serial numbers; Multiple serial numbers; Multiple serial numbers; Multiple serial numbers; Multiple serial numbers; Multiple serial numbers; Multiple serial numbers; Multiple serial numbers. Also covers: Mindray N Series Multiparameter Patient Monitoring System; TM 80 Telemetry device; Mindray BeneHeart C/D series AED - non rechargable; T1 Transport Monitor; iMEC Portable Patient Monitor; Mindray uMEC Patient monitor range; Mindray ePM Patient Monitor
- Reason
- The manufacturer has identified that the monitor manual contains insufficient descriptions regarding certain items, which may cause confusion for users., The monitor manual contains insufficient descriptions, which may cause confusion for users. To ensure consistency between the manual descriptions and device performance, the manufacturer will update the content below in the manual. It does not involve product design changes, it does not affect products' functionality or performance.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-08-06
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/8c65a1d1-7a21-453b-abcb-be8ef634b2ec