{
  "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": "2026-03-18",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Middletown",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "83200",
      "recalling_firm": "Geritrex, LLC",
      "address_1": "40 Commercial Ave",
      "address_2": "N/A",
      "postal_code": "10941-1444",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.A. Nationwide",
      "recall_number": "D-1521-2019",
      "product_description": "Ritussin DM Children & Adults, 4 Fl. Oz. (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10941, NDC 53807-409-04",
      "product_quantity": "5107 bottles",
      "reason_for_recall": "cGMP Deviations: Products may have microbial contamination.",
      "recall_initiation_date": "20190531",
      "center_classification_date": "20190725",
      "termination_date": "20240202",
      "report_date": "20190731",
      "code_info": "Lot #: 70602, Exp 6/19"
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}