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FDA urges docs to drop Getinge cardiac life support devices

FDA urges docs to drop Getinge cardiac life support devices
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Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

The latest Class I recall for these beleaguered devices relates to communication loss between circuit board assembly units.

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Getinge s Datascope has another serious aortic balloon pump recall

The FDA issued a notice determining a recall of Getinge subsidiary Datascope's Cardiosave IABPs as Class I, the most serious kind.

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Second Recall in Less Than 2 Months for Cardiosave IABPs

In a Class I recall notice, the FDA says a coiled cable that connects the display and the base may fail, causing the IABP to shut down.

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New IABP Recall: Balloon Catheter Damage Might Cause Bleeding Into Pump

This is the latest in a long string of recalls for the Getinge/Datascope Cardiosave Hybrid and Rescue IABPs.

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