{
  "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": "2026-07-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Wayne",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "62651",
      "recalling_firm": "Bayer HealthCare Pharmaceuticals Inc.",
      "address_1": "6 W Belt Plz",
      "address_2": "N/A",
      "postal_code": "07470",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Kansas and California.",
      "recall_number": "D-1433-2012",
      "product_description": "Estradiol Hemihydrate M20 EP/USP Powder, packaged in a) 1.5 kg and b) 2.5 kg fiber drums, Rx only, Art. No. 165811, Bayer Pharma AG, D-13342 Berlin.",
      "product_quantity": "112.295 kg",
      "reason_for_recall": "Cross Contamination w/Other Products: This active pharmaceutical ingredient is being recalled due to cross contamination with another product.",
      "recall_initiation_date": "20120508",
      "center_classification_date": "20120731",
      "termination_date": "20121218",
      "report_date": "20120808",
      "code_info": "Lot Number: 81202450, Exp 06/15/16"
    }
  ]
}