The Food and Drug Administration yesterday released an update on Medtronic’s recall of 1,614 devices used to pump blood from the heart to the rest of the body because the devices may malfunction. The notice updates affected models of the Heartware Ventricular Assist Device System and recommended actions. Medtronic initiated the recall in April due to a pump weld defect.

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The Food and Drug Administration has identified a Class I recall of certain convenience kits by AVID Medical that contain recalled Medline Namic Angiographic…
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The Food and Drug Administration has issued an early alert for all automated Impella controllers by Abiomed following an issue that has caused three deaths and…
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Boston Scientific, a large supplier of medical devices, said in an Aug. 26 statement posted on its website that on Aug. 25 it “identified a cybersecurity…
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The Food and Drug Administration has issued early alerts for the following products: •    Certain epidural kits by Medical Action…
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The Food and Drug Administration has identified a Class I recall of certain Medline convenience kits containing B. Braun components that have Huons Bupivacaine…
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The Food and Drug Administration Aug. 3 identified Class I recalls of two convenience kit products. Certain kits by Medline…