FDA Medical devices recall ·
WASPLab Product Name: WASPLab Model recall
- Recall number
- Z-2854-2026
- Date
- (initiated June 16, 2026)
- Company / brand
- Copan WASP
Via Achille Grandi, 32, Brescia, Italy - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 1
- Hazard tags
- Software
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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.
Why was it recalled?
Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2
Distribution
US Nationwide distribution in the state of Arizona.
States: Arizona
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2854-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.