Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: WebApp version 2.33.1, 2.33.3
Summary
The FDA issued a Class II for Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software by Copan WASP. Reason: Due to a software issue within the WebApp that potentially prevents the user to overwrite the results..
Details
Source
Device Recall
External ID
Z-2854-2026
Action Date
2026-08-12
Status
Ongoing
Category
device
Product Description
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.
Lot/Code Info: Lot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2
Quantity Affected: 1
Reason for Recall
Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.
Distribution
US Nationwide distribution in the state of Arizona.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-06-16
Company
Brescia
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 156 device recalls issued in the same week, part of 400 device-related FDA actions this month.
Copan WASP has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Copan WASP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Copan WASP have FDA actions?
Copan WASP has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-2854-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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