{
  "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": "2026-06-17",
    "results": {
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      "status": "Ongoing",
      "city": "Dayton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "99098",
      "recalling_firm": "Guardian Drug Co. Inc.",
      "address_1": "2 Charles Ct",
      "address_2": "",
      "postal_code": "08810-1508",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "distribution_pattern": "U.S.A. Nationwide",
      "recall_number": "D-0562-2026",
      "product_description": "Extra strength Antacid Calcium Carbonate 750 mg, chewable tablets, 96-count bottle, DISTRIBUTED BY CASEY'S MARKETING COMPANY, ANKENY, IA 50521, UPC: 0 98437 24361 9.",
      "product_quantity": "",
      "reason_for_recall": "Presence of foreign substance: small metallic particles in chewable tablets.",
      "recall_initiation_date": "20260528",
      "center_classification_date": "20260603",
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      "code_info": "Lot #: 1276118, Exp 1/31/2029.",
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