U.S. FDA classifies recall of Philips' respiratory devices as most serious https://ift.tt/N0DyZ6m

The U.S. health regulator said the silicon foam used in some reworked ventilator models may separate from plastic backing due to adhesive failure and can reduce the air flow as well as cause debris contamination. The company's ventilators provide breathing assistance to both pediatric and adult patients.

from Top Health News | Latest Health & Healthcare Industry Information and Updates: ET HealthWorld : ETHealthworld.com https://ift.tt/LmnRhBQ
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