{
  "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": "Harleysville",
      "address_1": "1499 Delp Dr",
      "reason_for_recall": "Product was packaged with the incorrect port and does not match the label.  The kit is labeled as an 8F Low Profile Pro-Fuse CT Port.  The kit contains an 8F Midsize Dignity CT Port.",
      "address_2": "",
      "product_quantity": "30",
      "code_info": "Catalog number MRCTT80041, Lot # MDNK860, Exp 02/2015",
      "center_classification_date": "20120626",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including the states of GA and WA and the countries of Ireland and Turkey.",
      "state": "PA",
      "product_description": "MRCTT80041 MedComp 8F Plastic Pro-Fuse(R) CT Low Profile Port with Attachable Chronoflex(R) Polyurethane Catheter.    Power Injectable Implantable Infusion Port insertion kit.",
      "report_date": "20120704",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medical Components, Inc dba MedComp",
      "recall_number": "Z-1868-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62238",
      "termination_date": "20130520",
      "more_code_info": "",
      "recall_initiation_date": "20120402",
      "postal_code": "19438",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}