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FDA Announces Nationwide Tylenol Recall—Thousands of Bottles Affected

A nationwide recall for about 3,000 bottles of Tylenol is underway, according to the Food and Drug Administration (FDA). The pain reliever was initially recalled in mid-October due to a “defective container,” and on Tuesday, the FDA gave the recall the second-highest risk level, Class II. This means taking the recalled medication may cause “temporary or medically reversible adverse health…