Drug recall
Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: WebApp version 2.33.1…
FDA recall event 99302 · Class II · Copan WASP
Key facts
| Event ID | 99302 |
|---|---|
| Recall numbers | Z-2854-2026 |
| Recalling firm | Copan WASP |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Due to a software issue within the WebApp that potentially prevents the user to overwrite the results. |
| Initiation date | Jun 16, 2026 |
| Report date | Aug 12, 2026 |
| City | Brescia |
| Country | Italy |
| FEI number | 3009288740 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: