{
  "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": "2026-04-15",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Durham",
      "address_1": "100 Rodolphe St",
      "reason_for_recall": "False Positive ESBL Phenotype",
      "address_2": "",
      "product_quantity": "30,292 cartons (20 cards per carton)",
      "code_info": "Ref: 421257 ALL LOTS",
      "center_classification_date": "20190216",
      "distribution_pattern": "UK and Ireland",
      "state": "NC",
      "product_description": "VITEK 2 AST-N351 Test Kit",
      "report_date": "20190227",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "bioMerieux, Inc.",
      "recall_number": "Z-0847-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81953",
      "termination_date": "20210816",
      "more_code_info": "",
      "recall_initiation_date": "20181213",
      "postal_code": "27712-9402",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}