{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Dover",
      "address_1": "87 Venture Drive",
      "reason_for_recall": "Defective component may cause extension sets to leak.",
      "address_2": "",
      "product_quantity": "3850",
      "code_info": "Lot Number:  1306034, 1307011",
      "center_classification_date": "20140123",
      "distribution_pattern": "US Nationwide Distribution in the states of: NY, VA, IL, MO, OR, FL, DE, OH",
      "state": "NH",
      "product_description": "AMS-530 7\u001d Microbore Trifurcated Extension sets      Product Usage:  Intravascular administration set.",
      "report_date": "20140129",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Churchill Medical Systems, Inc.",
      "recall_number": "Z-0813-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67255",
      "termination_date": "20141103",
      "more_code_info": "",
      "recall_initiation_date": "20140107",
      "postal_code": "03820-5914",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}