FDA Recall: Software Issue May Prevent User to Overwrite Results

Company: Copan WASP
Date of Enforcement Report: 7/31/2026
Class: II

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.

Recall Number:

Z-2854-2026

REASON:

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

RECALLING FIRM/MANUFACTURER:

Copan WASP

VOLUME:

DISTRIBUTION:

US Nationwide distribution in the state of Arizona.

About the author

Allison Pate

Allison joined SoftwareCPR in 2022, bringing along over ten years of passion for building teamwork and growth in organizations. This is established in part by the greatest University the South has to offer- Mississippi State.

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FDA Recall: Software Issue May Prevent User to Overwrite Results

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