{
  "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-0564-2026",
      "product_description": "MARKET BASKET ANTACID Calcium Carbonate 1000 mg, ULTRA STRENGTH, 72 Tablets, Distributed by: De Moules Supermarkets, Inc.,Tewksbury, Mass 01875,  UPC 0 49705 83149 6.",
      "product_quantity": "",
      "reason_for_recall": "Presence of foreign substance: small metallic particles in chewable tablets.",
      "recall_initiation_date": "20260528",
      "center_classification_date": "20260603",
      "report_date": "20260610",
      "code_info": "Lot #: 1716089, expires: JAN 2029.",
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