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.