{
  "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": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Morristown",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "77484",
      "recalling_firm": "Bayer HealthCare Pharmaceuticals, Inc.",
      "address_1": "36 Columbia Rd",
      "address_2": "N/A",
      "postal_code": "07960-4526",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1051-2017",
      "product_description": "Alka-Seltzer  Gold (1000 mg Anhydrous citric acid, 344 mg Antacid Potassium bicarbonate, 1050 mg Antacid Sodium bicarbonate/Antacid) Effervescent Tablets, 36-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981,  UPC 016500041085",
      "product_quantity": "56,064 36-count cartons",
      "reason_for_recall": "Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.",
      "recall_initiation_date": "20170330",
      "center_classification_date": "20170801",
      "termination_date": "20200108",
      "report_date": "20170809",
      "code_info": "BTAHGR0; Exp. 05/19  BTAHGR1; Exp. 05/19  BTAHGR2; Exp. 05/19  BTAJ0K3; Exp. 07/19"
    }
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}