Recall Z-1045-2022— Woodside Acquisitions Inc.
Class I · Ongoing
Class I FDA medical device recall by Woodside Acquisitions Inc., initiated 2022-04-09. FDA's recall record names no specific 510(k) clearance for this event. Product: Joysbio SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test. Reason: Firm distributed tests which have not been cleared or authorized for marketing or distribution in the United States..
- Recalling firm
- Woodside Acquisitions Inc.
- Classification
- Class I
- Status
- Ongoing
- Initiated
- 2022-04-09
- Firm location
- tyrone, PA, United States
Product description
Joysbio SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test
Reason for recall
Firm distributed tests which have not been cleared or authorized for marketing or distribution in the United States.
Data sourced from openFDA. This site is unofficial and independent of the FDA.