United StatesThe recalled product is the WASPLab automated device (Brand: WASPLab, Model/Catalog W087) running WebApp software versions 2.33.1, 2.33.3, or 2.34.2, used for incubation and digital imaging of agar culture plates. It was recalled because a software issue in the WebApp can potentially prevent the user from overwriting results; the recall was initiated by Copan WASP and affected distribution in the United States (state of Arizona).
What's being recalled
Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: WebApp version 2.33.1, 2.33.3 and 2.34.2 Product Description: WASPLab is an automated device intended to be used for the incubation and the digital imaging of agar culture plates streaked with microbiological specimens derived by the human body for microbiological investigations. WebApp software is the user interface of WASPLab device.
Recalling firm: Copan WASP, Brescia, Italy.
How to identify it
Lot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2
The hazard
Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.
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 Nationwide distribution in the state of Arizona.
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)