Z-2854-2026 Class II Ongoing
FDA device recall Z-2854-2026 was initiated by Copan WASP on June 16, 2026 and is designated Class II. Reason for recall: Due to a software issue within the WebApp that potentially prevents the user to overwrite the results. The recall status is ongoing. Affected quantity: 1.
Recall Details
- Product Type
- Devices
- Report Date
- August 12, 2026
- Initiation Date
- June 16, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1
Product Description
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 for Recall
Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.
Distribution Pattern
US Nationwide distribution in the state of Arizona.
Code Information
Lot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2