{
  "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-2933-2018",
      "product_description": "Double Lumen CRRT/ABP Catheter Set;  Hemodialysis catheter insertion kits, DL 11/15  DL 11/20  DL 9/15",
      "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": "MCAJ510 MCAP860 MCAZ820 MCCB890 MCCJ250 MCDF160  MCDQ630 MCFF200 MCFF620 MCFK200 MCFV440 MKAK310  MCAW770 MCBW430 MCCH320 MCCJ690 MCFB450 MCFF930  MCFV450 MKAK320 MKAV210  MCAY080 MCBD600 MCBP740  MCBW440 MCCA030 MCCH330"
    }
  ]
}