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FDA Recalls Mislabeled Medicine

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The company Qualitest Pharmaceuticals has issued a recall of tablets containing hydrocodone bitartrate and acetaminophen because they were incorrectly labeled as Phenobarbital.

No illnesses or injuries due to the mix-up have been reported. A nationwide recall of the product was issued, and the company and FDA do not believe that the mislabeled medicine has reached any stores around the country.

Pharmaceutical product defects like the mislabeling of products can cause severe illnesses and injuries. If you or a loved one has been the victim of pharmaceutical product defects, please contact the Stevens Point defective pharmaceutical products lawyers of Habush Habush & Rottier S.C. ® at 800-242-2874.