FDAFDA recall Z-2854-2026 · Aug 12, 2026
Copan WASP: Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: Web recall
Recall found
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.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Lot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2
- Quantity
- 1
- Distribution
- US Nationwide distribution in the state of Arizona.
- Recalling firm
- Copan WASP, Brescia
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-06-16
Source: openFDA enforcement record Z-2854-2026 · search recall number Z-2854-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.