{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Dover",
      "address_1": "87 Venture Dr",
      "reason_for_recall": "Incorrect priming volume printed on the device package.",
      "address_2": "",
      "product_quantity": "30,700",
      "code_info": "1610092D 1611091D 1612068D 1612074D",
      "center_classification_date": "20170318",
      "distribution_pattern": "US Nationwide Distribution in the states of NJ, TX, VA, FL, VA, MA, IL, MI, NY, OH, WA, PA, WV",
      "state": "NH",
      "product_description": "AMS-636, 60\" Microbore extension set.    Product Usage:  Accessory devices used to administer medical fluids.",
      "report_date": "20170329",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.",
      "recall_number": "Z-1484-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76607",
      "termination_date": "20190422",
      "more_code_info": "",
      "recall_initiation_date": "20170220",
      "postal_code": "03820-5914",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}