Woodside Acquisitions recalls all Joysbio SARS-CoV-2 Antigen Rapid Test Kits (Colloidal Gold) sold in the U.S. due to lack of FDA clearance. These unapproved tests may not work correctly.
Firm distributed tests which have not been cleared or authorized for marketing or distribution in the United States.
Woodside Acquisitions is recalling all units of the Joysbio SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) because they were not cleared by the FDA for sale in the U.S. This means the tests could be inaccurate and not meet safety standards.
The tests were distributed without being cleared or authorized by the FDA for use in the United States. This means they might not work properly and could lead to incorrect test results, such as false negatives or positives.
Anyone who purchased the Joysbio SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) from Woodside Acquisitions. People using these tests for home COVID-19 testing may get inaccurate results.
Check for the product name 'Joysbio SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold)' and the manufacturer 'Woodside Acquisitions Inc.' on the packaging. All lots are affected.
Look for the product name and manufacturer on the packaging to confirm if it's the recalled item.
The tests were distributed without being cleared or authorized by the FDA for marketing or distribution in the United States.
All lots of the Joysbio SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) are affected.
The recall record does not specify a remedy, so no action is required beyond checking if you have the product.
We’ve drafted a message you can send Woodside Acquisitions Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-1045-2022 — Woodside Acquisitions Inc. Woodside Acquisitions Inc. Hello, I own a Woodside Acquisitions Inc. that is covered by recall Z-1045-2022 from Woodside Acquisitions Inc.. 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.
