Penumbra is initiating a voluntary Field Removal of the original version of Neuron 6F 070 Delivery Catheter. For these catheters, Penumbra has received feedback from some users that the catheter could kink or ovalize in certain anatomical situations.
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Penumbra Announces Worldwide Voluntary Field Removal of the Original Version of 6F Neuron 070 Delivery Catheter
FDA Consumer Health Information Updates: New Web Videos Educate Consumers about Food and Medical Product Safety
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FDA Consumer Health Information Updates: New Web Videos Educate Consumers about Food and Medical Product Safety
CareFusion Corporation, which is expected to become a public company following its planned spinoff from Cardinal Health, today issued the following update regarding its previously disclosed recall of the Alaris System: On June 12, 2009, the company sent an urgent Medical Device Recall Notification to customers of its Alaris® System addressing potential risks identified with the Alaris System.
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Carefusion Issues Update Regarding Previously Disclosed June 12, 2009 Recall of the Alaris®