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.

Class II

Recalling firm: Copan WASP
Reason for recall: Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.
Affected products (lot / model / serial): Lot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2
Units affected: 1
Distribution pattern: US Nationwide distribution in the state of Arizona.
Firm location: Brescia, Italy
Recall type: Voluntary: Firm initiated
How the firm notified customers: Letter
Product type: Devices
Status: Ongoing
Recall number: Z-2854-2026
Recall initiated: June 16, 2026
FDA classification date: July 31, 2026
FDA report date: August 12, 2026
FDA event ID: 99302
Last updated on HTM Vibe: August 18, 2026