{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Harleysville",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80581",
      "recalling_firm": "Medical Components, Inc dba MedComp",
      "address_1": "1499 Delp Dr",
      "address_2": "N/A",
      "postal_code": "19438-2936",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide distribution; worldwide distribution.",
      "recall_number": "Z-2934-2018",
      "product_description": "Duo-Flow Double Lumen Soft Tip CRRT/ABP Catheter Set; DL11/24  . Hemodialysis catheter insertion kits",
      "product_quantity": "N/A",
      "reason_for_recall": "The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious injury or death.",
      "recall_initiation_date": "20180712",
      "center_classification_date": "20180825",
      "termination_date": "20200702",
      "report_date": "20180905",
      "code_info": "MCAL840 MCBB800 MCBW450 MCCH690"
    }
  ]
}