{
  "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": [
    {
      "status": "Terminated",
      "city": "Detroit",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "68209",
      "recalling_firm": "Caraco Pharmaceutical Laboratories, Ltd.",
      "address_1": "1150 Elijah McCoy Dr",
      "address_2": "N/A",
      "postal_code": "48202-3344",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "OH",
      "recall_number": "D-1407-2014",
      "product_description": "Gemcitabine For Injection USP, 1 g, (lyophilized), For Intravenous Use Only, Sterile Single Use Vial, Rx only, Manufactured by: Sun Pharmaceutical Ind. Ltd, Gujarat, India, NDC 47335-154-40",
      "product_quantity": "200 vials",
      "reason_for_recall": "Lack of Assurance of Sterility: A particle excursion for a different batch of the same product may lead to a lack of sterility assurance.",
      "recall_initiation_date": "20140409",
      "center_classification_date": "20140620",
      "termination_date": "20140929",
      "report_date": "20140702",
      "code_info": "JKM7188A"
    }
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}