FDA Recalls Levothyroxine Nationwide: What You Need to Know
Food and Drug Administration (FDA). The nationwide recall involves multiple dosage strengths of Levothyroxine Sodium Tablets packaged in 10-count blister packs. Levothyroxine Sodium Tablets Recall Details and Classifications According to the FDA, the recall was initiated on July 13 and designated as a Class II on July 17. A Class II designation indicates that the … Read more