Woodside Acquisitions recalls all Oral Rapid SARS-CoV-:2 Antigen Rapid Test Kits sold in the US as they are unapproved for marketing. Consumers should not use these tests.
Firm distributed tests which have not been cleared or authorized for marketing or distribution in the United States.
Woodside Acquisitions is recalling all Oral Rapid SARS-CoV-2 Antigen Rapid Test Kits sold in the US because they were not cleared or authorized for marketing by the FDA. This means the tests could be unsafe for use.
The tests were distributed without being cleared or authorized by the FDA for use in the United States. Using unapproved tests could lead to inaccurate results or potential health risks.
Anyone who purchased or uses the Oral Rapid SARS-CoV-2 Antigen Rapid Test Kit from Woodside Acquisitions. People who rely on these tests for COVID-19 screening are at risk of using unapproved products.
The product is labeled 'Oral Rapid SARS-CoV-2 Antigen Rapid Test Kit' or 'COVID 19 Test' from Woodside Acquisitions. All lots are affected, so no specific model or date is needed.
Immediately stop using the Oral Rapid SARS-CoV-2 Antigen Rapid Test Kit as it is unapproved for US marketing.
No, these tests were not cleared or authorized by the FDA for marketing in the US, so they are unsafe for use.
The product is labeled 'Oral Rapid SARS-CoV-2 Antigen Rapid Test Kit' or 'COVID 19 Test' from Woodside Acquisitions. All lots are affected.
Immediately stop using it and do not use the product as it is unapproved for US marketing.
We’ve drafted a message you can send Woodside Acquisitions to request your refund or repair — edit it as you like.
Subject: Recall Z-1044-2022 — Woodside Acquisitions Woodside Acquisitions Hello, I own a Woodside Acquisitions that is covered by recall Z-1044-2022 from Woodside Acquisitions. 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.
