{
  "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": "74452",
      "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 states of AL; CA; CO; FL; KY; MA; NY; OH; SC; TX; UT; VA and WI.",
      "recall_number": "Z-2282-2016",
      "product_description": "Instructions for Use (IFU) for Progesterone 3 Calibrator Set, repackaged as one set/package.       The Instructions for Use (IFU) included in the package was for the incorrect lot number. Only the IFU required correction.",
      "product_quantity": "41 single sets of Progesterone 3 calibrators",
      "reason_for_recall": "Instructions For Use had incorrect lot number and calibrator values",
      "recall_initiation_date": "20160607",
      "center_classification_date": "20160725",
      "termination_date": "20170222",
      "report_date": "20160803",
      "code_info": "Catalog Number 02534001 (One set of Calibrators US)    Lot G13C303 (only those received/repackaged in the US)"
    }
  ]
}