The Food and Drug Administration last week alerted health care providers and patients that batteries in certain Medtronic implantable pacemakers and cardiac resynchronization therapy pacemakers may drain more quickly than expected without warning. The devices provide pacing for slow heart rhythms and heart failure. FDA said it has received three reports of the batteries draining early because of a crack in the device’s capacitor, resulting in one patient’s death. FDA recommends that providers advise their patients to continue to use their remote monitors, which can be set to alert the patient and provider when the battery level drops below a certain limit, and to immediately replace the device if they receive such a notice.
 

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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…