{
  "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": "Antioch",
      "address_1": "3034 Owen Dr",
      "reason_for_recall": "Sealant on the base trim of sterilizer container may be deteriorated or absent which could provide a path for contaminants to enter the container under certain conditions post-sterilization.",
      "address_2": "",
      "product_quantity": "38 units",
      "code_info": "All",
      "center_classification_date": "20170111",
      "distribution_pattern": "Worldwide Distribution",
      "state": "TN",
      "product_description": "symmetry surgical ULTRA(R) Gravity container, REF numbers:  C131310-G, C13134-G, C13135-G, C13136-G, C13139-G, C13854-G, C13855-G, C13856-G, C181310-G,  C18134-G, C18135-G, C18136-G, C18138-G, C22854-G,   C22855-G, C22856-G, C22858-G, C24134-G, C24135-G, C24136-G,  C24138, C24138-G    Product Usage:  sterilization container",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Symmetry Surgical, Inc.",
      "recall_number": "Z-1012-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75850",
      "termination_date": "20170820",
      "more_code_info": "",
      "recall_initiation_date": "20161129",
      "postal_code": "37013-2413",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}