Ventavis Recall Announced by FDA
A partial recall of Ventavis / iloprost, a drug marketed by Actelion Pharmaceuticals US, Inc. for the treatment of Pulmonary Arterial Hypertension (PAH), or Primary Pulmonary Hypertension (PPH). Ventavis is an inhalation solution that comes in glass ampules.
Ventavis Recalled Lots
The Ventavis recall was announced after Actelion received numerous reports that some ampules were empty or contained less than the full amount of Vantavis. This manufacturing defect can result in a person with PAH or PPH receiving too little medication, which can be potentially fatal. The recalled lots of Ventavis/iloprost are Lots #63228A, #63230A, #63231A and #63232A.
Ventavis Recall Lawsuit
If you or a friend of loved one has been injured or died as a result of receiving one of the recalled lots of Ventavis, please contact the Willis Law Firm to discuss a possible product liability lawsuit due to the defective / recalled Ventavis. As discussed above, the incorrect amount of Ventavis / iloprost can cause serious personal injury or death.
Call and discuss your Ventavis Recall Lawsuit with a Board Certified Personal Injury Trial Lawyer, certified by the Texas Board of Legal Specialization since 1988. Get a Free & Confidential Lawsuit Evaluation by calling us at 1-800-883-9858 or e-mailing us here.