{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Fairfield",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "95944",
      "recalling_firm": "Akron Pharma, Inc.",
      "address_1": "373 Us Highway 46 Ste 117",
      "address_2": "",
      "postal_code": "07004-2456",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the US",
      "recall_number": "D-0195-2025",
      "product_description": "Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.",
      "product_quantity": "14825 bottles",
      "reason_for_recall": "Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.",
      "recall_initiation_date": "20241212",
      "center_classification_date": "20250110",
      "report_date": "20250122",
      "code_info": "Lot #s: KDT0124004, KDT0124005, KDT0124006, Exp 08/31/2026",
      "more_code_info": ""
    }
  ]
}