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FDA and Penumbra Inc. Recall Catheter
On May 29, 2009, the Food and Drug Administration and Penumbra Inc. notified healthcare workers that a Class I recall was beginning for the Penumbra Neuron 5F Select Catheter.
FDA and Penumbra Inc. Recall Catheter
On May 29, 2009, the Food and Drug Administration and Penumbra Inc. notified healthcare workers that a Class I recall was beginning for the Penumbra Neuron 5F Select Catheter.