Copan Italia recalls 1ml of DTT in liquid phase
- Recalling company
- Copan Italia
- Product
- 1ml of DTT in liquid phase, in PET tube with capture cap, in bulk
- Reason
- Treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Oct 29, 2025
- Reported
- Dec 24, 2025
- Distribution
- US Distribution to states of: CA, CO, FL, GA, MN, MS, NH, NJ, NY, OH, PA, TN, TX, UT
- Status
- Ongoing
- Quantity
- 122,850 units US
- Lot / codes
- UDI:0U020N.A - (01)18053326005043
- Company location
- Brescia
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0943-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0943-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.