CELLEX Photopheresis Kit recall — FDA Z-1822-2026
Increased difficulty in installing the centrifuge bowl onto the centrifuge bowl holder. Improper installation may cause the centrifuge bowl to dislodge, resulting in a broken bowl during…
Overview of recall records associated with THERAKOS DEVELOPMENT LIMITED, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Increased difficulty in installing the centrifuge bowl onto the centrifuge bowl holder. Improper installation may cause the centrifuge bowl to dislodge, resulting in a broken bowl during…
This page summarizes recall records in which the official source identifies THERAKOS DEVELOPMENT LIMITED 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.