Synthroid Lawyer Helping Victims
The Food and Drug Administration (FDA) said today that Knoll Pharmaceutical Company is recalling certain Synthroid tablets because of mis-packaging. 100 mcg product was packaged into 200 mcg card.
This is the first public notice of this Class II recall issued by FDA.
If you or loved one have been injured as a result of taking the above drug, you may have a valid claim. Call us now at 1-(800) 888-8888 or contact us.