[Recalled] Joysbio SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test — Firm distributed tests which have not been cleared or authorized for marketing… | FDA 2022-04-09
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | Joysbio SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test |
|---|---|
| Brand / manufacturer | Woodside Acquisitions Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1045-2022 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 09 April 2022 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Firm distributed tests which have not been cleared or authorized for marketing or distribution in the United States.
This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
Related recalls from Woodside Acquisitions Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.