Copan Italia 1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum recall — FDA Z-0942-2026
Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.
Overview of recall records associated with Copan Italia, including dates, categories and classifications where available.
Classification mix: Class II: 2.
Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.
Treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.
This page summarizes recall records in which the official source identifies Copan Italia 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.