{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Bloomington",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90800",
      "recalling_firm": "American Contract Systems, Inc.",
      "address_1": "4801 W 81st St",
      "address_2": "N/A",
      "postal_code": "55437-1111",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution to one customer in PA only",
      "recall_number": "Z-0071-2023",
      "product_description": "COVID Test Kit Nonsterile",
      "product_quantity": "39,575 kits",
      "reason_for_recall": "Kit incorrectly labeled for use with COVID testing and should not be used with any SARS-Co-V2 device.",
      "recall_initiation_date": "20220812",
      "center_classification_date": "20221008",
      "report_date": "20221019",
      "code_info": "1) UDI-DI: Product Code: AHCV18A, Lots 980221 (exp. 01/20/2023) and 974221 (exp. 01/25/2023)  2) UDI-DI: Product Code: AHCV18B, Lots 868221 (exp. 05/31/2023), 842221 (exp. 05/31/2023)"
    }
  ]
}