{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Lansdale",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64458",
      "recalling_firm": "Vygon Corporation",
      "address_1": "2750 Morris Rd Ste A200",
      "address_2": "N/A",
      "postal_code": "19446-6083",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was distributed to 4 hospitals (under one hospital network) within the State of Pennsylvania",
      "recall_number": "Z-0937-2013",
      "product_description": "Churchill Medical Systems, Inc. A Vygon Company - All sizes of CMS-CT6T225 6F Triple Lumen CT PICC with M.S.T. Components, Peripherally Inserted Central Catheter.",
      "product_quantity": "210",
      "reason_for_recall": "Product was packaged with the incorrect introducer needle.  The kit label indicates a \"safety\" needle is included; the kits were packaged with a non-safety needle.",
      "recall_initiation_date": "20121217",
      "center_classification_date": "20130311",
      "termination_date": "20140114",
      "report_date": "20130320",
      "code_info": "Lots numbers MBKQ640, exp 05/2015; MBKZ720, exp 05/2015; MBLJ290, exp 06/2015; MBLR100, exp 07/2015; MBLZ350, exp 09/2015; and MBMG250, exp 10/2015.",
      "more_code_info": ""
    }
  ]
}