{
  "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": "Canonsburg",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "71218",
      "recalling_firm": "Mylan Lab Inc",
      "address_1": "1500 Corporate Dr Ste 400",
      "address_2": "N/A",
      "postal_code": "15317-8580",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1111-2015",
      "product_description": "Mycophenolic Acid Delayed-release Tablets, 180 mg, 120-count bottle, Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 U.S.A., NDC 0378-4201-78, UPC 3 0378-4201-78 7.",
      "product_quantity": "7,722 bottles",
      "reason_for_recall": "Failed Dissolution Specifications: Low out of specification dissolution results.",
      "recall_initiation_date": "20150520",
      "center_classification_date": "20150529",
      "termination_date": "20161021",
      "report_date": "20150610",
      "code_info": "Lot #: 3059043, Exp 08/16"
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