THERAKOS CELLEX Photopheresis Procedural Kit PRODUCT CODE: CLXUSA recall — FDA Z-0212-2022
Product was released prior to all testing being completed. If used and a drive tube leak were to occur, may cause illness or injury.
Overview of recall records associated with Therakos, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Product was released prior to all testing being completed. If used and a drive tube leak were to occur, may cause illness or injury.
This page summarizes recall records in which the official source identifies Therakos, 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.