{
  "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": "Rochester",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66900",
      "recalling_firm": "Ortho-Clinical Diagnostics",
      "address_1": "100 Indigo Creek Dr",
      "address_2": "N/A",
      "postal_code": "14626-5101",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide distribution - all states.",
      "recall_number": "Z-0557-2014",
      "product_description": "VITROS Anti-HBs Calibrators & VITROS Anti-HBs Reagent Packs",
      "product_quantity": "1,920 kits",
      "reason_for_recall": "Ortho Clinical Diagnostics issued a Product Correction Notification for VITROS Immunodiagnostic Products Anti-HBs Calibrators and Anti-HBs Quantitative Reagent Packs due to false positive results.",
      "recall_initiation_date": "20131025",
      "center_classification_date": "20131220",
      "termination_date": "20180518",
      "report_date": "20140101",
      "code_info": "Product Code 1) 6801926, 2) 6801925, 3) 6802452  Lot numbers: 1) 6700, 2) 6731, 3) 6830  Expiry Dates: 1) 21 May 2013, 2) 24 July 2013, 3) 11 Sept 2013",
      "more_code_info": ""
    }
  ]
}