{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Pasadena",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87682",
      "recalling_firm": "INNOVA MEDICAL GROUP, INC.",
      "address_1": "800 E Colorado Blvd Ste 200",
      "address_2": "N/A",
      "postal_code": "91101-5401",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - U.S. Nationwide in the states of AL, AZ, CA, CO, CT, DC, DE, FL, GA, IL, IN, KY, MA, MD, ME, MI, MN, MO, NC, NE, NH, NJ, NV, NY, OH, PA, RI, TN, TX, UT, VA, VT, WA, and WI. The countries of Canada, India and United Kingdom.",
      "recall_number": "Z-1539-2021",
      "product_description": "COVID-19 Self-Test Kit *** INNOVA *** 3T",
      "product_quantity": "402 boxes (=1,206 tests)",
      "reason_for_recall": "Due to distributing test kits to customers who were not part of a clinical investigation.",
      "recall_initiation_date": "20210409",
      "center_classification_date": "20210610",
      "report_date": "20210616",
      "code_info": "Catalog Number: 3T  Lot Numbers:  U2102003  X2012310"
    }
  ]
}