Wond: Unauthorized distribution of Clarity Strep A Rapid Test Kits for home use poses risks. Recall covers specific model numbers and lot numbers. Consumers should check if they have these kits and contact Wondfo for details.
Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device would include sales and distribution of this test for at-home use, non-prescription use, over-the-counter use, or direct-to-consumer customers.
Wondfo is recalling Clarity Strep A Rapid Test Kits due to unauthorized distribution. These kits were sold for home use without proper authorization, which could lead to unsafe testing practices.
Unauthorized distribution means these test kits were sold for home use without proper authorization. This could lead to incorrect results or unsafe testing practices if used without medical guidance.
Anyone who purchased the Clarity Strep A Rapid Test Kits with the specified model numbers and lot numbers from unauthorized sellers. Home users testing for strep A without medical supervision are most at risk.
Check for model numbers CD-STP25 or CD-STP25V with specific lot numbers listed in the recall notice. These kits were sold through unauthorized channels for home use.
Identify if your kit has model numbers CD-STP25 or CD-STP25V with the listed lot numbers.
Wondfo identified unauthorized distribution of these test kits for home use, which could lead to unsafe testing practices.
Model numbers CD-STP25 and CD-STP25V with specific lot numbers listed in the recall notice.
The recall does not specify a remedy, so contact Wondfo directly for details.
We’ve drafted a message you can send Wondfo to request your refund or repair — edit it as you like.
Subject: Recall Z-2031-2024 — Wondfo Wondfo Hello, I own a Wondfo that is covered by recall Z-2031-2024 from Wondfo. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
