{
  "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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    {
      "country": "United States",
      "city": "Elkton",
      "address_1": "125 Blue Ball Rd",
      "reason_for_recall": "Presence of natural rubber latex is not declared in the label",
      "address_2": "",
      "product_quantity": "12 packs",
      "code_info": "Lot Numbers: V A30",
      "center_classification_date": "20190227",
      "distribution_pattern": "TX",
      "state": "MD",
      "product_description": "Cardiovascular Procedure Kit (CLR MP4 COIL 2 SPIKE)  Catalog Number: 140222",
      "report_date": "20190306",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Terumo Cardiovascular Systems Corporation",
      "recall_number": "Z-0966-2019",
      "initial_firm_notification": "Letter",
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      "recall_initiation_date": "20181220",
      "postal_code": "21921-5315",
      "voluntary_mandated": "Voluntary: Firm initiated",
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