{
  "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-2941-2018",
      "product_description": "DUO FLOW CUSTOM TRAYS; TRAY #414  TRAY #415  TRAY #67",
      "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": "MCBC900 MCBP350 MCDC900 MCGA140    MCCD760 MKAL320      MCAS020 MCCF310 MCCV750 MCCV870 MCDL720 MCDV440  MCFJ760 MKAF680"
    }
  ]
}