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Recall Observatory FDA recall evidence

Device product

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

Z-3308-2024

June 26, 2024

Class II

Product summary

Firm
FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN)CO.,LTD
Event
Event 95288
Status
Ongoing
Classification
Class II
Quantity
50,000 kits
Official record key
device-enforcement:Z-3308-2024

Official wording

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

Code information: All lots in the United States

Distribution pattern: International distribution to the countries of China and Hong Kong.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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