{
  "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": "2026-08-19",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 2
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Lindon",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Food",
      "event_id": "98325",
      "recalling_firm": "TKS Co-pack Manufacturing, LLC",
      "address_1": "2642 W 400 N Ste 700",
      "address_2": "N/A",
      "postal_code": "84042-1142",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distributed to customer in Utah.",
      "recall_number": "H-0520-2026",
      "product_description": "Aonic Complete Hers. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in plastic bottle, induction sealed closed with plastic lid. Each bottle is a serving intended to be taken orally as a dietary supplement. Shipping unit: two 15 count decorated boxes in a corrugated Aonic Master Shipper.  Firm Name and Address on Label: Aonic Inc. 2261 MarketStreet #5416 San Francisco, CA 94114 USA.",
      "product_quantity": "3630 individual bottles",
      "reason_for_recall": "Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.",
      "recall_initiation_date": "20260115",
      "center_classification_date": "20260220",
      "report_date": "20260218",
      "code_info": "Lot 5349A BB 12/27;  Lot 5363A BB 12/27"
    }
  ]
}