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Home › FDA recalls › Brand Name: WASPLab Product Name: WASPLab
CLASS II · ModerateFDA

Copan WASP recalls Brand Name: WASPLab Product Name: WASPLab

📅 Jun 16, 2026 · 📍 Nationwide
Recalling company
Copan WASP
Product
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.
Reason
Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
Jun 16, 2026
Reported
Aug 12, 2026
Distribution
US Nationwide distribution in the state of Arizona.
Status
Ongoing
Quantity
1
Lot / codes
Lot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2
Company location
Brescia
Recall type
Voluntary: Firm initiated
Recall number
Z-2854-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-2854-2026 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.