{
  "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": "tyrone",
      "state": "PA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89975",
      "recalling_firm": "SML Distribution, LLC",
      "address_1": "1500-1631 Lincoln Ave.",
      "address_2": "N/A",
      "postal_code": "16686",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide distribution in the states of AL, FL, GA, MO, NY, TX, and WY.",
      "recall_number": "Z-0944-2022",
      "product_description": "Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test",
      "product_quantity": "209,450 units",
      "reason_for_recall": "The product was distributed without FDA authorization or clearance for marketing and distribution in the US.",
      "recall_initiation_date": "20220304",
      "center_classification_date": "20220503",
      "report_date": "20220511",
      "code_info": "All lots:  UL-AG-2110-05-Q UL-AG-2111-02-Q UL-AG-2112-01-Q UL-AG-2112-02-Q UL-AG-2201-03-Q"
    }
  ]
}