Wond: Unauthorized distribution of Strep A rapid test kits for home use poses safety risks. Affected kits include Easy Healthcare Corporation and Areta Strep A Swab Test products.
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 recalls certain Strep A rapid test kits sold for home use because they were distributed without authorization. This unauthorized distribution means the kits could be sold to non-prescription customers, increasing the risk of improper use.
Unauthorized distribution of these test kits means they could be sold to non-prescription customers, leading to improper use. This increases the risk of incorrect results or misuse without medical guidance.
People who purchased the recalled Strep A test kits from unauthorized sellers or non-prescription sources are affected. Those using these kits without medical supervision are at higher risk.
Check for product labels: Easy Healthcare Corporation, Areta Strep A Swab Test, or EASY at Home Medical LLC. Lot numbers E03920802 are part of the recalled kits.
Look for labels indicating Easy Healthcare Corporation, Areta Strep A Swab Test, or EASY at Home Medical LLC.
Wondfo identified unauthorized distribution of the Preview Strep A Test Kit for home use, which could be sold to non-prescription customers.
Streptococcal A rapid test kits labeled as Easy Healthcare Corporation, Areta Strep A Swab Test, or EASY at Home Medical LLC with lot number E03920802.
Check the product label for the brand names mentioned and the specific lot number E03920802.
We’ve drafted a message you can send Wondfo to request your refund or repair — edit it as you like.
Subject: Recall Z-2032-2024 — Wondfo Wondfo Hello, I own a Wondfo that is covered by recall Z-2032-2024 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.
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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.
