Class II
Medical Device Recall: 1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum transfer device, for WASP* *Compatible with Copan s WASP (Walk-Away Specimen Processor for Microbiology) System
Copan Italia · October 29, 2025
Reason for Recall
Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.
Distribution
US Distribution to states of: CA, CO, FL, GA, MN, MS, NH, NJ, NY, OH, PA, TN, TX, UT
States Affected
CA, CO, FL, GA, MN, MS, NH, NJ, NY, OH, PA, TN, TX, UT
Quantity Affected
122,850 units US
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0942-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.