{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Irving",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76868",
      "recalling_firm": "Mentor Texas, LP.",
      "address_1": "3025 Skyway Cir N",
      "address_2": "N/A",
      "postal_code": "75038-3524",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : MI, CA, CT, IL, IN, NY, NC, OH and OK.",
      "recall_number": "Z-2070-2017",
      "product_description": "Mentor Smooth Round SPECTRUM Post-  Operatively Adjustable Saline Breast Implant, Product Code: 350-1490, UDI/GTIN: 00081317002048",
      "product_quantity": "28 units",
      "reason_for_recall": "Missing Dome Pack accessory.",
      "recall_initiation_date": "20170327",
      "center_classification_date": "20170511",
      "termination_date": "20170613",
      "report_date": "20170517",
      "code_info": "Lot Number: 7377332"
    }
  ]
}