{
  "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": "2026-06-10",
    "results": {
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  "results": [
    {
      "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",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.A. Nationwide",
      "recall_number": "D-0570-2026",
      "product_description": "Harris Teeter, ULTRA STRENGTH ANTACID, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, Distributed by: Harris Teeter, LLC.,MATTHEWS, NC 28105, UPC: 0 72036-73108-1.",
      "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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    }
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}