Copan Wasp: Calculator/data Processing Module, For Clinical Use
Recall Summary Copan WASP is recalling WASPLab automated microbiology devices with specific software versions (2.33.1, 2.33.3, and 2.34.2) because a software issue may prevent users from correcting or overwriting test results. The recall affects devices distributed nationwide across all U.S. states and the District of Columbia. This is classified as a serious recall (Class I).
- Recalling firm
- Copan WASP
- 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.
- Classification
- Class I
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-06-16
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the state of Arizona.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/76aa74c9-aa53-453f-93d8-1fce5869c8ce