{
  "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": "2026-07-29",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Bridgewater",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "92407",
      "recalling_firm": "Kramer Laboratories, Inc.",
      "address_1": "440 Us Highway 22 Ste 210",
      "address_2": "N/A",
      "postal_code": "08807-2477",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "nationwide within the United States",
      "recall_number": "D-0943-2023",
      "product_description": "Safe Tussin PM Night Time Cough Relief (Cough Suppressant/Antihistamine), packaged in 4.0 FL OZ(118mL) bottles, Kramer Laboratories, Inc. Bridgewater, NJ 08807",
      "product_quantity": "N/A",
      "reason_for_recall": "CGMP Deviations: use of non-food grade lubricant in mixing vessel.",
      "recall_initiation_date": "20230623",
      "center_classification_date": "20230724",
      "termination_date": "20240312",
      "report_date": "20230802",
      "code_info": "Lot #: 8639, Exp. Date 8/2023"
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}