{
  "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": "Brecksville",
      "state": "OH",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86828",
      "recalling_firm": "Applied Medical Technology Inc",
      "address_1": "8006 Katherine Blvd",
      "address_2": "N/A",
      "postal_code": "44141-4202",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, GA, IL, MA, MO, PA, TX, VA. No foreign distribution.",
      "recall_number": "Z-0698-2021",
      "product_description": "AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter, Model Number ETRN102.     Box PN TRN102, Box UDI (01)00842071109066(17)230901(10)200918-103, Pouch PN ETRN102, Pouch UDI (01)00842071108007(17)230901(10)200902-075",
      "product_quantity": "N/A",
      "reason_for_recall": "The products subject to this recall may contain obvious, incorrect pouch labels while the outer box has the correct label.",
      "recall_initiation_date": "20201110",
      "center_classification_date": "20201223",
      "termination_date": "20210903",
      "report_date": "20201230",
      "code_info": "Box Lot Number 200918-103; Pouch Lot Number 200902-075"
    }
  ]
}