{
  "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,
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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-1050-2017",
      "product_description": "Alka-Seltzer Extra Strength (500 mg Aspirin (NSAID), 1985 mg Analgesic Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric Acid) Effervescent Tablets, 24-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981,  UPC 016500044048",
      "product_quantity": "24,672 24-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": "BTAHDG0; Exp. 04/19"
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}