RecallRadar

FDA Device recall Z-2854-2026

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 Des…

On 2026-08-12 the FDA classified a Class II recall of 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 Des… by Copan Wasp, citing due to a software issue within the WebApp that potentially prevents the user to overwrite the results.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2854-2026
ClassificationClass II
Statusongoing
Initiated2026-06-16
Published2026-08-12
Last updated2026-09-13 11:58 UTC
CompanyCopan Wasp
DistributionUS

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.

Reason

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

Identifiers

code_infoLot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2854-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.