{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Harlan",
      "state": "IA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98469",
      "recalling_firm": "Molded Products Inc",
      "address_1": "1812 Industrial Pkwy",
      "address_2": "",
      "postal_code": "51537-2401",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of TN, TX, NV, IL, FL.",
      "recall_number": "Z-1774-2026",
      "product_description": "See Luer Cap Set, MPC-130, set, administration, intravascular",
      "product_quantity": "26900 units",
      "reason_for_recall": "Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.",
      "recall_initiation_date": "20260217",
      "center_classification_date": "20260406",
      "report_date": "20260415",
      "code_info": "UDI +B144MPC1300/$$529105203895, Lot Number 20389",
      "more_code_info": ""
    }
  ]
}