Philips recalled certain magnetic resonance imaging (MRI) systems because of the risk of machines exploding. The Food and Drug Administration labeled the action as a Class I recall. In November, ...
An innovative tech company has recently unveiled Recall, a groundbreaking AI-driven platform designed exclusively for summarizing online content. Recall stands out with its browser extension that ...
Feb 15 (Reuters) - The U.S. FDA said on Thursday it has classified a recall of Philips' medical imaging machines as "most serious" due to the risk of a detector falling unexpectedly in some devices.
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