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Medical Device Network on MSNFDA tags Medtronic embolisation device recall as Class IThe US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as ...
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Medical Device Network on MSNFDA tags Becton, Dickinson and Company infusion software recall as Class IProblematic software has been the cause of multiple infusion pump recalls in the medical device industry over the past few ...
The U.S. Food and Drug Administration issued a Class II recall notice to take back 8,242 cases (197,808 cans) of Good & ...
Class II recalls — a grade below the most serious Class I recalls — reference a situation in which the use of or exposure to ...
XBeta founder Frederick Kruger offers advice for medical device startups based on his firm's development of the Spiro Wave ...
The FDA recall affects more than 25,000 of the Fridley-run company’s devices and follows reports of 17 injuries.
More than 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) ...
A drug dealer was arrested after he accidentally exposed his identity with a photo of just his fingers. Kane Molyneux has now ...
THE Food and Drug Administration (FDA) has launched an online application process for Certificate of Medical Device ...
We have written at length about the U.S. Food and Drug Administration’s (FDA’s) actions to promulgate regulations specifying the agency’s authority ...
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