{
  "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": "South San Francisco",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71493",
      "recalling_firm": "Tosoh Bioscience, Inc.",
      "address_1": "6000 Shoreline Ct Ste 101",
      "address_2": "N/A",
      "postal_code": "94080-7606",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Us Nationwide Distribution in the state ID including PR.",
      "recall_number": "Z-2066-2015",
      "product_description": "G7 Variant Elution Buffer HiS no. 1 (M) component of the Tosoh Automated Glycohemoglobin Analyzer HLC 723G7.     Product Usage:  G7 Variant Elution Buffer HiS No 1. (M) is one of the buffers used on Tosoh Automated Glycohemoglobin Analyzer HLC 723G7.",
      "product_quantity": "9 boxes/5 pouches",
      "reason_for_recall": "The G7 Variant Elution Buffer HiS no. 1 (M) is incorrectly labeled with an expiration date of October 2015.  The correct expiration date is October 2014.",
      "recall_initiation_date": "20150210",
      "center_classification_date": "20150714",
      "termination_date": "20151001",
      "report_date": "20150722",
      "code_info": "Catalog # 021446, Lot # H7-111W, Exp. Date 10-2015",
      "more_code_info": ""
    }
  ]
}