{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "North Brunswick",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Food",
      "event_id": "87745",
      "recalling_firm": "Church & Dwight Co., Inc. OGI Distribution Center",
      "address_1": "2300 Us Highway 1",
      "address_2": "N/A",
      "postal_code": "08902-4438",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The product was distributed thru out the US and Canada, Panama, China,",
      "recall_number": "F-0462-2021",
      "product_description": "vitafusion Fiber Well 220ct, 10 / 220 CT",
      "product_quantity": "2928 Bottles",
      "reason_for_recall": "Potential presence of a metallic mesh material in products.",
      "recall_initiation_date": "20210419",
      "center_classification_date": "20210428",
      "termination_date": "20220203",
      "report_date": "20210505",
      "code_info": "Product Code: 027917019840  Lot Codes: WA03087520, WA02487524, WA03086273",
      "more_code_info": ""
    }
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}