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Splitting Tips Spur Class I Recall For Cook's Beacon Tip Angiographic Catheter

FDA designated Cook Medical's recall of its Beacon Tip angiographic catheters in early July as a class I action. The catheters’ show a tendency to split or separate from the catheter, which could cause serious injury to patients, FDA said.

At least 2,239 lots of Cook Medical Inc.’s Beacon Tip angiographic catheters were recalled on July 2, leading to an Aug. 10 "class I" recall designation by FDA.

The company said in an Aug. 3 notice

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