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Another Headache For Philips As Company Recalls Millions Of Sleeping Masks

Magnets In The Masks Can Interfere With Other Implanted Devices

 
• By Brian Bossetta

The US FDA says a Philips recall of more than 17 million masks worn with some recalled breathing machines raises further safety concerns about other medical devices manufactured by the company.

Product Recall Dart
• Source: Shutterstock

After recalls of its sleep apnea breathing devices, Royal Philips is now recalling the some of the masks that go with them.

The Food and Drug Administration has issued another safety alert pertaining to Philips Respironics, a Philips subsidiary, notifying patients and providers that the company has recalled more than 17...

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Industry Execs Talk Tariff Turbulence During MD&M East

 
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More from Policy & Regulation

Zika Virus Test Among 4 New FDA Device Classifications

 
• By Elizabeth Orr

The FDA plans to announce class II status for four new device types, including tests for the Zika virus and genetic condition Fragile X. This follows earlier announcements and highlights a trend toward diagnostic classifications. The classifications are considered deregulatory, meaning they will hel

FDA Draft Guidance Introduces Electric Submission For Q-Sub Process

 
• By Brian Bossetta

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• By Brian Bossetta

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