{
  "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": [
    {
      "country": "United States",
      "city": "Dover",
      "address_1": "87 Venture Dr",
      "reason_for_recall": "The Iodine Prep Pads within the Vygon IV Start Convenience Kits, had stability samples that were not meeting iodine assay level requirements to support the 36 month expiration date.  All kits containing the affected pads were recalled.",
      "address_2": "",
      "product_quantity": "21350",
      "code_info": "AMS-623T-6 (1506075D, 1508057D, 1511030D, 1604024D, 1605080D, 1610017D, 1706097D, 1707055D) and AMS-626TGSLF (1601102D, 1603099D, 160581D, 1607019D, 1610057D, 1703068D, 1703069D, 1704065d, 1706076D, 1707031d, 1707056D)",
      "center_classification_date": "20180309",
      "distribution_pattern": "US Distribution.",
      "state": "NH",
      "product_description": "Vygon IV Start Convenience Kits; Product Codes AMS-623T and AMS-626TGSLF.     Kit used when administering IV during emergency.",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.",
      "recall_number": "Z-0933-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79318",
      "termination_date": "20200106",
      "more_code_info": "",
      "recall_initiation_date": "20171003",
      "postal_code": "03820-5914",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}