{
  "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": "Tijuana",
      "state": "N/A",
      "country": "Mexico",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75273",
      "recalling_firm": "Surgical Specialties Mexico S DE RL DE CV",
      "address_1": "Corredor Tijuana - Rosarito 2000-24702 B",
      "address_2": "Ejido Francisco Villa",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: OH, PA, CO, MA, DE, CA, NY, VA, WA, NJ, CT, FL, TX, NH, ID, OK, AZ, GA, PA, NV, VT.    Worldwide: Spain, Italy, United Kingdom, Portugal, Turkey, Germany, Denmark,",
      "recall_number": "Z-0068-2017",
      "product_description": "BioSentry Tract Sealant System, Product Code: 768022019S; Indicated to provide accuracy in marking a biopsy location for visualization during surgical resection.",
      "product_quantity": "512 boxes (2560 units)",
      "reason_for_recall": "Surgical Specialties Mexico is recalling the BioSentry Track Sealant System due to the potential for an open seal on the product package.",
      "recall_initiation_date": "20160924",
      "center_classification_date": "20161011",
      "termination_date": "20161206",
      "report_date": "20161019",
      "code_info": "MAWX380, MAZD460, MAZR350, MBCF540"
    }
  ]
}