{
  "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": "Harleysville",
      "address_1": "1499 Delp Dr",
      "reason_for_recall": "The kit was packaged with the incorrect guidewire. The label indicates the kit contains a marked guidewire. The kits were packaged with an unmarked guidewire.",
      "address_2": "",
      "product_quantity": "24 Eaches",
      "code_info": "Lot/Serial/Model/Catalog Numbers/Exp. Date:   Lot # MJKK420;   serial # N/A,   Catalog # MRDP80PLN,   Exp. Date 2022-01-09;   UDI#- 884908110449",
      "center_classification_date": "20180329",
      "distribution_pattern": "CA, AR. AL",
      "state": "PA",
      "product_description": "8F Plastic Dignity¿ Low Profile CT Port W/Pre-Attached ChronoFlex¿ Polyurethane Catheter",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medical Components, Inc dba MedComp",
      "recall_number": "Z-1271-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79445",
      "termination_date": "20180711",
      "more_code_info": "",
      "recall_initiation_date": "20171122",
      "postal_code": "19438-2936",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}