Class II — Copan WASP
| Recalling firm | Copan WASP |
|---|---|
| Classification | Class II |
| Status | Ongoing |
| Reason | Due to a software issue within the WebApp that potentially prevents the user to overwrite the results. |
| 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. |
| Quantity | 1 |
| Distribution | US Nationwide distribution in the state of Arizona. |
| Initiated | 2026-06-16 |
| Classified | 2026-07-31 |
| Recall number | Z-2854-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Copan WASP (Z-2854-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99302/
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