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Recall Observatory FDA recall evidence

Device product

Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) 20 TESTS/1 KIT Green and white box under the brand DiagnosUS, and, White box without brand name labeled as "SARS -COV-2 ANTIGEN DEVELOPMENT MADE IN USA ORAL SWAB TESTING

Z-0929-2023

November 28, 2022

Class I

Product summary

Firm
Universal Meditech Inc.
Event
Event 91321
Status
Ongoing
Classification
Class I
Quantity
56,300 kits
Official record key
device-enforcement:Z-0929-2023

Official wording

Reason: Distribution of SARS-CoV-2 Antigen Rapid Test Kits without FDA market approval, clearance or Emergency Use Authorization.

Code information: Model Number: 550-10 UDI Code: None Lot Numbers: UL-AG-2111-01-Q UL-AG-2111-02-Q UL-AG-2110-05-Q UL-AG-2112-02-Q UL-AG-2110-03-Q UL-AG-2110-04-Q

Distribution pattern: U.S. Nationwide distribution in the states of CA, and TX.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Distribution of SARS-CoV-2 Antigen Rapid Test Kits without FDA market approval, clearance or Emergency Use Authorization.