Lower risk Medical device recall · FDA · Published June 16, 2026

WASPLab W087 Software Version 2.33.1/2.33.3/2.34.2: Potential Data Overwrite Issue

WASPLab W087 devices with WebApp versions 2.33.1, 2.33.3, and 2.34.2 may prevent overwriting results. Consumers should check their software version and contact support for updates.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2854-2026Medical device WASPLab ›

Lower-risk recall

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

✎ GovInfoNow plain-language explainer

WASPLab W087 devices with specific WebApp software versions could prevent users from overwriting results. This might cause data loss if the device is used for microbiological testing. Read more at govinfonow.com/recall/314349-wasplab-w087-software-version-2-33-1-2-33-3.

Source Summary by GovInfoNow · govinfonow.com/recall/314349-wasplab-w087-software-version-2-33-1-2-33-3 · Updated August 18, 2026 · FDA enforcement record: FDA #Z-2854-2026

Cite this page

“WASPLab W087 Software Version 2.33.1/2.33.3/2.34.2: Potential Data Overwrite Issue.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/314349-wasplab-w087-software-version-2-33-1-2-33-3. Based on FDA recall #Z-2854-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2854-2026%22&limit=1).

The FDA announced on June 16, 2026, that Copan WASP is recalling WASPLab software versions 2.33.1, 2.33.3, and 2.34.2 due to a potential inability to overwrite results. The agency issued recall number Z-2854-2026 for the Class II voluntary recall.

How to tell if you have it

Brand: WASPLab
Product Name: WASPLab
Model/Catalog Number: W087
Software Version: WebApp version 2.33.1, 2.33.3 and 2.34.2

The hazard

According to the FDA, a software issue within the WebApp potentially prevents the user from overwriting results. The recall is classified as Class II.

Context

GovInfoNow's records show Copan WASP has one other recall on record since May 6, 2025. On May 6, 2025, the company issued a recall for PhenoMATRIX Software due to potential inaccurate patient diagnosis risks.

How to tell if you have this one

Check your WASPLab device's WebApp version. Versions 2.33.1, 2.33.3, and 2.34.2 are affected.

Brand
WASPLab
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Software Version
Look for the WebApp version on your WASPLab device to see if it is 2.33.1, 2.33.3, or 2.34.2.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “US Nationwide distribution in the state of Arizona.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 57 days after the firm started it.

Jun 16, 2026Firm started the recall
Jul 31, 2026FDA classified it Class II
Aug 12, 2026Published in FDA’s Enforcement Report
Aug 18, 2026Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

Similar recalls

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Keep exploring

More WASPLab recalls

Link to this recall

<a href="https://govinfonow.com/recall/314349-wasplab-w087-software-version-2-33-1-2-33-3">WASPLab W087 Software Version 2.33.1/2.33.3/2.34.2: Potential Data Overwrite Issue (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2854-2026 (June 16, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2854-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.