U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company was added by ICIJ.
The parent company information is based on 2017 public records.
데이터 추가 비고
Percutaneous catheter - Product Code DQY
원인
Misbranding--some products may be identified with the wrong id band content 'neuron 6f 070' instead of 'neuron 6f delivery'.
조치
Firm initiated its recall on June 30, 2009. Consignees notified on July 6 and 7, with follow up contact on July 7, 2009. Contact Penumbra Inc. at 1.510.618.3223, if there are any questions.
CA, FL, NC, MI, MO, VA, AZ, CT, IA, NY, and CO, Foreign: Germany and Australia.
제품 설명
Penumbra Neuron Delivery Catheter 053, 115 cm/12 cm-- MP, manufactured by Penumbra Inc., Alameda, CA || Percutaneous Catheter, indicated for the introduction of interventional devices into the peripheral, coronary and neuro vasculature.