Actelion Pharmaceuticals U.S Ventavis (iloprost) Inhalation Solution, 10 mcg/1 mL, Sterile recall — FDA D-143-2013
Subpotent Drug: OOS (out of specification) assay result at the 12 month stability time point.
Overview of recall records associated with Actelion Pharmaceuticals U.S., Inc., including dates, categories and classifications where available.
Classification mix: Class III: 1.
Subpotent Drug: OOS (out of specification) assay result at the 12 month stability time point.
This page summarizes recall records in which the official source identifies Actelion Pharmaceuticals U.S., Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.