{
  "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-0196-2025",
      "product_description": "Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for:  Akron Pharma Inc., 373 US RT 46 W Building E, Suite 117, Fairfield, NJ 07034, NDC 71399-8022-02",
      "product_quantity": "1232 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: KDT0224001B, Exp 08/31/2026; KDT0224002B, Exp 09/30/2026.",
      "more_code_info": ""
    }
  ]
}