{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Dover",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78951",
      "recalling_firm": "Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.",
      "address_1": "87 Venture Dr",
      "address_2": "N/A",
      "postal_code": "03820-5914",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "U.S.",
      "recall_number": "Z-0681-2018",
      "product_description": "19Ga x 1  Huber Needle Set. Product Code:  MBS-1910.",
      "product_quantity": "156",
      "reason_for_recall": "Vygon is conducting a voluntary recall of the products and lots listed in this recall, being  initiated because our Tyvek supplier has notified Vygon of issues with their product, specifically the  Tyvek may not be coated completely causing gaps in the adhesive used to seal the product packaging.  This potential lack of adhesive may affect the sterility of the product.",
      "recall_initiation_date": "20170724",
      "center_classification_date": "20180221",
      "termination_date": "20191107",
      "report_date": "20180228",
      "code_info": "Lot Number: 1706049D"
    }
  ]
}