Recall Z-2854-2026— Copan WASP
Class II · Ongoing
Class II FDA medical device recall by Copan WASP, initiated 2026-06-16. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Copan WASP
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-06-16
- Firm location
- Brescia, Italy
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.