Xelstrym (dextroamphetamine) transdermal system, 13.5 mg dextroamphetamine/9 hours, 30 recall — FDA D-0055-2025
Defective Delivery System: The product does not meet predetermined specifications for Coldflow (adhesive).
Overview of recall records associated with Noven Pharmaceuticals Inc, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Defective Delivery System: The product does not meet predetermined specifications for Coldflow (adhesive).
This page summarizes recall records in which the official source identifies Noven Pharmaceuticals 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.