Urgent Field Safety Notice For Rotaflow Console By Maquet Cardiopulmonary Ag

Rotaflow Console Recall Summary Maquet Cardiopulmonary AG has issued a Class I urgent field safety notice for the Rotaflow Console, a medical device used in cardiac procedures. The notice was distributed to facilities in Germany and the EU, indicating a serious safety concern with the device. The specific reason for the recall is not detailed in the available information.

Recalling firm
Maquet Cardiopulmonary AG
Product
Rotaflow Console
Reason
Urgent Field Safety Notice for Rotaflow Console by Maquet Cardiopulmonary AG
Classification
Class I
Category
medical device recall
Country
Germany
Agency
BFARM
Recall date
2026-10-27
Status
Ongoing
Distribution
Germany / EU

Official recall notice from BFARM

Recall details on Nibble Recalls: https://trynibble.app/recalls/2bf98a39-40bd-4ada-a72a-f96a3bfbfb8a