Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087… — Class II medical device recall Z-2854-2026
Ongoing recall by Copan WASP, reported 2026-08-12, distributed nationwide. Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.
| Recall number | Z-2854-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Copan WASP, Brescia, Italy |
| Recall initiated | 2026-06-16 |
| Classified | 2026-07-31 |
| Reported by FDA | 2026-08-12 |
| Distributed | Nationwide (US) |
| Quantity | 1 |
| Reason classes | software |
| Model numbers | W087 |
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 for recall
Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2854-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.