{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Middlesex",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "65889",
      "recalling_firm": "Core Pharma Llc",
      "address_1": "215 Wood Ave",
      "address_2": "N/A",
      "postal_code": "08846-2554",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1062-2013",
      "product_description": "Pyridostigmine Bromide Tablets 60 mg, USP Rx Only 100 Tablets, Manufactured and Distributed by: CorePharma, LLC Middlesex, NJ 08846 NDC 64720-128-10  NDC 64720-128-10",
      "product_quantity": "960 bottles",
      "reason_for_recall": "Failed Stability Specifications: Pyridostigmine Bromide tablets, is being recalled due to an out of specification test result during stablity testing.",
      "recall_initiation_date": "20130702",
      "center_classification_date": "20130920",
      "termination_date": "20140825",
      "report_date": "20131002",
      "code_info": "109497; Exp. 12/15"
    }
  ]
}