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Other links at Articles > Cardiology |
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Class I Recall of Penumbra Reperfusion Catheter 032
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FDA has now determined that a recall of Penumbra catheters for mid-shaft joint failures is a Class I recall, the most serious kind. The recall began with direct customer contact October 28. Medscape Medical News
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Pill Burden Too Great in Dialysis Patients?
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In this video blog, Jeffrey Berns, MD, of UPenn School of Medicine, discusses a study which looks at the large number of pills that dialysis patients must take. Medscape Nephrology
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