Fresh Recalls

FDAClass II · Medical device · Recall Z-2854-2026 · Recalled August 12, 2026

Brand Name recall — Copan WASP

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Brand Name
Company / brand
Copan WASP
Lot / serial / date codes
Lot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2
Distribution
US Nationwide distribution in the state of Arizona.
Agency product description and boundaries

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.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Brand Name

3. Open the official notice or contact

Official recall ID
Z-2854-2026
Brand
Copan WASP
Classification
Class II
Units affected
1
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Brescia, Italy
Firm address
Via Achille Grandi, 32, N/A

Identifying details (verbatim from the notice)

Product codes / lots
Lot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2
Distribution
US Nationwide distribution in the state of Arizona.
Firm notified the public via
Letter
FDA event ID
99302
Recall initiated
June 16, 2026
FDA classified
July 31, 2026
FDA report date
August 12, 2026
Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

Report a data error on this page