UPDATE: Risk of Device Failures for Getinge’s Maquet/Datascope Cardiosave Intra-Aortic Balloon Pump (IABP) – Letter to Health Care Providers

FDA Recalls · 2024-05-08T04:00:00+0000

Cardiosave IABP devices may unexpectedly shutdown or interrupt therapy (pump stops). View the full article

By FDA Recalls
May 8, 2024 in Recalls

Join the conversation

You can post now and register later. If you have an account, sign in now to post with your account.

Reply to this topic...

Only 75 emoji are allowed.

× Your link has been automatically embedded. Display as a link instead

× Your previous content has been restored. Clear editor

× You cannot paste images directly. Upload or insert images from URL.