Urgent Field Safety Notice For Beneheart D1 By Shenzshenzhen Mindray Bio-medical Electronics Co., LTD
Recall Summary BeneHeart D1 defibrillators manufactured by Shenzhen Mindray Bio-Medical Electronics have been recalled in Germany and the EU due to a safety issue. This is classified as a Class I recall, indicating a serious problem. The recall notice requires corrective field actions to address the identified risk.
- Recalling firm
- Urgent Field Safety Notice for BeneHeart D1 by SHENZSHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD , Download_Veroeff
- Product
- s Tasks of the BfArM Risk assessment Field corrective actions Urgent Field Safety Notice for BeneHeart D1 by SHENZSHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO
- Reason
- assessment Field corrective actions Urgent Field Safety Notice for BeneHeart D1 by SHENZSHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO
- Classification
- Class I
- Category
- medical device recall
- Country
- Germany
- Agency
- BFARM
- Recall date
- 2026-06-11
- Status
- Ongoing
- Distribution
- Germany / EU
Official recall notice from BFARM
Recall details on Nibble Recalls: https://trynibble.app/recalls/a44afcb2-0a30-4afe-9090-83d943c6564b