{
  "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": [
    {
      "country": "United States",
      "city": "South San Francisco",
      "address_1": "6000 Shoreline Ct Ste 101",
      "reason_for_recall": "The label contains two different methodologies. Quality Control values for non-FDA approved methodology (CL) are on the label in addition to the FDA approved methodology values (AIA). Two sets of instructions were included on the label.",
      "address_2": "",
      "product_quantity": "64 boxes",
      "code_info": "TgAb: G644899 Expires June 2017; G844801 Expires August 2017 & GX44802 Expires 09/30/2017.",
      "center_classification_date": "20170526",
      "distribution_pattern": "Product was shipped to the following states: AK, FL, GA, MA, NY, NY, OH, OK & TX.",
      "state": "CA",
      "product_description": "AIA-PACK TgAb CONTROL SET",
      "report_date": "20170607",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Tosoh Bioscience, Inc.",
      "recall_number": "Z-2169-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76659",
      "termination_date": "20190208",
      "more_code_info": "",
      "recall_initiation_date": "20170208",
      "postal_code": "94080-7606",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}