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US FDA classifies recall of heart devices by Getinge as most serious

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US FDA classifies recall of heart devices by Getinge as most serious

The U.S. Food and Drug Administration (FDA) on Friday classified the recall of Getinge AB's heart devices as the most serious type, saying their use may cause injuries or death.

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US FDA classifies recall of heart devices by Getinge as most serious

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US FDA classifies recall of heart devices by Getinge as most serious

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