{
  "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": [
    {
      "status": "Terminated",
      "city": "Antioch",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64962",
      "recalling_firm": "Symmetry Medical/SSI",
      "address_1": "3034 Owen Dr",
      "address_2": "N/A",
      "postal_code": "37013-2413",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA including CA, MS, FL, PA, TN, CO, IL, TX, OH, MI, MA, IL and internationally to  Belgium, Canada, Germany, UK",
      "recall_number": "Z-1267-2013",
      "product_description": "Codman(R) Collins Radioparent Sternal Blade Nylon,4 3/4\" (121 mm) long,  3\" (76 mm) wide, 1 1/2\" (38 mm) deep, REF 50-8081    sternum retractor",
      "product_quantity": "524 boxes of 10",
      "reason_for_recall": "There is a possibility that the Collins Radioparent Sternal Blades Nylon may break during use.",
      "recall_initiation_date": "20130410",
      "center_classification_date": "20130507",
      "termination_date": "20140512",
      "report_date": "20130515",
      "code_info": "244576, 244582, 244584, 268916, 268920, 276513, 276514, 296136, 296139, 296141, 296153, 296155, 296156, 296157, 296160"
    }
  ]
}