{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Indianapolis",
      "address_1": "9402 Uptown Dr Ste 1100",
      "reason_for_recall": "Labeling: Not elsewhere classified. NDC number is incorrect on the container.",
      "address_2": "",
      "product_quantity": "40 Bottles",
      "code_info": "Lot # NW 46400021, Exp 03/2018",
      "center_classification_date": "20151202",
      "distribution_pattern": "Nationwide",
      "state": "IN",
      "product_description": "Prednisone 20 mg, Tablet, 10-count bottle, Rx only, Mfg by: HIKMA Pharmaceuticals PO BOX 182400 Amman 11118 Jordan. Dist By: West-Ward Pharmaceuticals Corp., Eatentown, NJ 07724 USA, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46256. NDC 51655-320-53",
      "report_date": "20151209",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Northwind Pharmaceuticals LLC",
      "recall_number": "D-0485-2016",
      "initial_firm_notification": "E-Mail",
      "product_type": "Drugs",
      "event_id": "72647",
      "termination_date": "20170329",
      "more_code_info": "",
      "recall_initiation_date": "20151110",
      "postal_code": "46256-1042",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}