FDA Classifies Cough Drops Recall as Moderate Risk Due to Quality Concerns
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FDA Classifies Cough Drops Recall as Moderate Risk Due to Quality Concerns

What's Happening? The U.S. Food and Drug Administration (FDA) has classified a nationwide recall of multiple cough drop products as a Class II recall, indicating a moderate risk to consumers. The recall, initiated on March 20, 2026, was prompted by an FDA inspection at an overseas manufacturing faci
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