{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Philadelphia",
      "state": "PA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "71836",
      "recalling_firm": "Mutual Pharmaceutical Company,  Inc.",
      "address_1": "1100 Orthodox St",
      "address_2": "N/A",
      "postal_code": "19124-3168",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1421-2015",
      "product_description": "Felodipine Extended-Release Tablets,  5 mg, 100 count bottles,  Rx only, Mutual Pharmaceutical Co. Inc., Philadelphia, PA --- NDC 53489-369-01",
      "product_quantity": "97,859 bottles",
      "reason_for_recall": "Chemical Contamination; benzophenone leached from the product label varnish",
      "recall_initiation_date": "20150716",
      "center_classification_date": "20150909",
      "termination_date": "20161013",
      "report_date": "20150916",
      "code_info": "lot #s: 6662801 & 6662901, exp 10/15, 6689601, exp 4/16, 6689701, exp 5/16 and 6708401, 8/16"
    }
  ]
}