Medical Device Network on MSN7d
FDA 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 ...
Medical Device Network on MSN5d
FDA 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 & ...
XBeta founder Frederick Kruger offers advice for medical device startups based on his firm's development of the Spiro Wave ...
THE Food and Drug Administration (FDA) has launched an online application process for Certificate of Medical Device ...
Class II recalls — a grade below the most serious Class I recalls — reference a situation in which the use of or exposure to ...
There were 1,048 medical device recalls in 2024, an increase of almost 25% from the 840 recalls that occurred in 2023, according to the Food and Drug Administration. Class I recalls, the most ...
South Wales Argus on MSN4d
Man arrested over class A drug offences following early-morning raidA man has been arrested over a series of drug offences following a successful early morning warrant carried out by police ...
More than 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) ...
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 ...
Medtronic will remove one model of Pipeline Vantage devices from where they’re used and sold and will update the instructions ...
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