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Home » More Than 1M Boston Scientific Recalled Angiographic Catheters Deemed Class I by FDA
More Than 1M Boston Scientific Recalled Angiographic Catheters Deemed Class I by FDA
A recall of more than 1 million Boston Scientific angiographic catheters from certain batches has been considered Class I by the FDA due to an increase in complaints about an inability to advance the guidewire through the lumen of the device for certain batches.