{
  "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": "Columbus",
      "state": "OH",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "65457",
      "recalling_firm": "American Health Packaging",
      "address_1": "2550 John Glenn Ave",
      "address_2": "Suite A",
      "postal_code": "43217-1188",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-892-2013",
      "product_description": "buPROPion Hydrochloride Extended Release Tablets, USP 100 mg, 100 count carton, 10 blister cards of 10 individually blistered and labeled tablets, Rx only, Actavis South Atlantic LLC, Packaged and Distributed by: American Health Packaging, Columbus, OH --- NDC 68084-470-01",
      "product_quantity": "389 cartons",
      "reason_for_recall": "Failed Stability Specifications; out of specification results at the 9 month stability time point for color, dissolution and related compounds.",
      "recall_initiation_date": "20130204",
      "center_classification_date": "20130815",
      "termination_date": "20130828",
      "report_date": "20130821",
      "code_info": "The following codes are affects by the recall:  Lot #114500, Exipration Date 08/2013, repackaging date 12/04/2011.",
      "more_code_info": ""
    }
  ]
}