{
  "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": "Durham",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88844",
      "recalling_firm": "bioMerieux, Inc.",
      "address_1": "100 Rodolphe St",
      "address_2": "N/A",
      "postal_code": "27712-9402",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution in WI, NY, and SD",
      "recall_number": "Z-0243-2022",
      "product_description": "API 50 CH, Model 50300",
      "product_quantity": "1382 kits",
      "reason_for_recall": "There is potential to provide an incorrect organism identification.",
      "recall_initiation_date": "20210930",
      "center_classification_date": "20211117",
      "termination_date": "20240118",
      "report_date": "20211124",
      "code_info": "Model 50300, Lot 1008679230    UDI: (01)03573026087401  (17)220330  (10)1008679230",
      "more_code_info": ""
    }
  ]
}