{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Trumbull",
      "address_1": "75 Corporate Dr",
      "reason_for_recall": "A diaphragm size 80 labeled box was incorrectly packaged with a size 85.",
      "address_2": "",
      "product_quantity": "200 units",
      "code_info": "Lot 153309",
      "center_classification_date": "20150618",
      "distribution_pattern": "AK, CA, DC, FL, IL, ME, MT, NE, NJ, NM, NY, OK, OR, P A, VA, W A, and WI  Foreign: CANADA, ENGLAND, and POLAND",
      "state": "CT",
      "product_description": "MILEX OMNIFLEX DIAPHRAGM SIZE 80  Model: MXWF80",
      "report_date": "20150624",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "CooperSurgical, Inc.",
      "recall_number": "Z-1814-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71329",
      "termination_date": "20160120",
      "more_code_info": "",
      "recall_initiation_date": "20150520",
      "postal_code": "06611-1350",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}