Recall Ledger

Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software... recall (Copan WASP)

Medical deviceClass IIOngoing

Summary: Copan WASP is recalling 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 . Reason: Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.

What is being recalled

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

Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US Nationwide distribution in the state of Arizona. (states named: Arizona)

How to tell if yours is affected

Lot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-2854-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedJune 16, 2026
ReportedAugust 12, 2026
CompanyCopan WASP
Company locationBrescia, Italy
Initiated byVoluntary: Firm initiated
Quantity1

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