United States1 ml DTT in liquid phase supplied in PET tubes with capture caps, sold in bulk and with a sputum transfer device and compatible with Copan’s WASP (Walk-Away Specimen Processor for Microbiology) System (UDI: 0U020N.A - (01)18053326005036; 0U020N.A - (01)18053326005043) is affected. It was recalled because treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.
What's being recalled
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
1ml of DTT in liquid phase, in PET tube with capture cap, in bulk
Recalling firm: Copan Italia, Brescia, Italy.
How to identify it
UDI:0U020N.A - (01)18053326005036 UDI:0U020N.A - (01)18053326005043
The hazard
Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.
Treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Distribution to states of: CA, CO, FL, GA, MN, MS, NH, NJ, NY, OH, PA, TN, TX, UT
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)