medical MODERATE Updated 2026-08-12

Copan WASP recalls Brand Name: WASPLab Product Name: WASPLab Model/Catalog Nu

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Recalled 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.

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Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

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View official government recall

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