{
  "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": "Kansas City",
      "state": "MO",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90324",
      "recalling_firm": "American Contract Systems, Inc.",
      "address_1": "2610 Ne Industrial Dr Ste 220",
      "address_2": "N/A",
      "postal_code": "64117-2648",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution in the state of Minnesota.",
      "recall_number": "Z-1277-2022",
      "product_description": "Nasopharyngeal sample collection tray for COVID-19 testing, labeled as COVID TEST KIT NONSTERILE 184312, AHCV18A",
      "product_quantity": "274,400 kits total",
      "reason_for_recall": "Affected products were assembled off-site by individuals who may not have been properly trained.",
      "recall_initiation_date": "20220502",
      "center_classification_date": "20220701",
      "report_date": "20220713",
      "code_info": "UDI-DI: 00191072121233   Lots: 721211, 672211, 657211, 994221, 980221, 974221",
      "more_code_info": ""
    }
  ]
}