Please provide your email address to receive an email when new articles are posted on . Datascope/Maquet/Getinge intra-aortic balloon pumps recalled due to risk for unexpected shutdown. The FDA has ...
The US Food and Drug Administration (FDA) today issued a letter to healthcare providers describing a current shortage of Getinge intra-aortic balloon pump (IABP) catheters and other components.
Following 12 company recalls and nearly 3,000 reported issues related to its cardiovascular life support systems since January 2023, Getinge has now drawn more scrutiny from the FDA — as the agency ...
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