FDA recall record

FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN)CO DVOT SARS-CoV-2 & RSV &MP &ADV & FIu A/B recall — FDA Z-3308-2024

The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.

Class IIclassification
Z-3308-2024official record ID
Oct 9, 2024report date

Recall record at a glance

Official recordZ-3308-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmFENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN)CO., LTD
Report dateOct 9, 2024
Recall initiation dateJun 26, 2024
Quantity50,000 kits
LocationShenzhen, N/A, China

Official product description

DVOT SARS-CoV-2 & RSV &MP &ADV & FIu A/B Antigen Combo Test Kit, Model Number ACT01

Why the product was recalled

The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.

Distribution information

International distribution to the countries of China and Hong Kong.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.