{
  "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": "Terminated",
      "city": "Irwindale",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89676",
      "recalling_firm": "WHPM Inc.",
      "address_1": "5358 Irwindale Ave Ste B",
      "address_2": "",
      "postal_code": "91706-2086",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: CA, FL, LA, MA and TX    O.U.S.: N/A",
      "recall_number": "Z-0892-2022",
      "product_description": "First SIGN  SARS-CoV-2 Antigen Test",
      "product_quantity": "535,755 tests",
      "reason_for_recall": "Frm became aware that a customer complaint was reported to US FDA that SARS-CoV-2 Antigen Tests were sold domestically by a pharmacy in California.  These Antigen Tests have not received FDA Emergency Use Authorization, nor have these tests been cleared or approved by FDA for commercial distribution in the U.S.",
      "recall_initiation_date": "20220304",
      "center_classification_date": "20220407",
      "termination_date": "20250205",
      "report_date": "20220413",
      "code_info": "Model Number: FSSA-CK20  UDI Codes:  None  Lot Numbers:  F0301214078;  F1227210039;  F0809210004;  F0906210010;  P0211214070;  F0914210014;  F1013210020;  F1214210034;  F0121220041;",
      "more_code_info": ""
    }
  ]
}