Penumbra Recalls Faulty Catheter

Penumbra is recalling its Neuron 5F Select Catheter, an action the FDA considers a Class I recall. The product is used to remove blood clots or foreign objects from blood vessels. The devices were distributed between May 5 and June 12 and are being recalled because they may contain pin holes and exposed wire braids, which could result in a brain clot or blood vessel puncture and lead to possible death, according to an FDA statement.