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Philips said in a statement it had flagged the matter with the FDA itself after a review Philips conducted over the past three months that found 270 complaints over the over the past three years.
Jun. 15—Medical equipment company Philips has issued a recall on some products to address possible health risks associated with a foam component meant to help reduce noise. The polyester-based ...
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During the pandemic, Philips conducted a series of studies on the foam, showing the deteriorating foam and chemicals released by it, which could cause "serious injury, life-threatening or permanent impairment". [2] The company said patients' health is its top priority, and regretted the "distress and concern" that the recall caused.
Philips was recalling the ventilators after detecting contaminants such as dust and dirt from the environment in the air path of some devices. The company has received 542 reports about this issue ...
FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.
AMSTERDAM (Reuters) -The U.S. Food and Drug Administration (FDA) said it is still not satisfied with how Dutch healthcare technology company Philips has handled a major product recall and the ...
The plot was loosely adapted into the 1990 film Total Recall, directed by Paul Verhoeven and starring Arnold Schwarzenegger. A remake was directed by Len Wiseman and released on August 3, 2012. While the owners of Carolco had licensed the story from Dick for the 1990 version, the 2012 film was largely based on the original and does not credit ...
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