FDA’s Class I recall of ResMed’s respiratory devices due to product labelling correction, not product removal, Top Health News | Latest Healthcare Sector & Healthcare Industry news, Information and Updates: ET HealthWorld : ETHealthworld.com

Food and Drug Administration’s recent issuance of a Class I recall acknowledges this classification is due to a correction of the product’s labelling and not a product removal. Anything contrary is incorrect and should be corrected to ensure the correct information reaches consumers: ResMed spokesperson, Food and Drug Administration’s recent issuance of a Class I recall acknowledges this classification is due to a correction of the product’s labelling and not a product removal. Anything contrary is incorrect and should be corrected to ensure the correct information reaches consumers: ResMed spokesperson, , Read More