The manufacturer has identified that certain Abiomed heart pumps with differential pressure sensors have the potential to display inaccurate information.

Johnson & Johnson’s Abiomed has sent an urgent medical device correction about a malfunction risk linked to 22 reports of serious injuries. The Food and Drug Administration, which published an early ...

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The agency says there have been 22 injuries and no deaths associated with this potentially high-risk device issue.

The FDA has issued an early alert warning of a potentially high-risk issue affecting certain Abiomed heart pumps. The agency said Abiomed issued an urgent medical device correction Jan. 27 for all ...

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