{
  "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": [
    {
      "country": "United States",
      "city": "Columbus",
      "address_1": "2550 John Glenn Ave Ste A",
      "reason_for_recall": "Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule",
      "address_2": "",
      "product_quantity": "761 cartons",
      "code_info": "Lot 152418, exp. 12/31/16, lot 153544, exp. 3/31/17, lot 154835, exp. 5/31/17",
      "center_classification_date": "20160902",
      "distribution_pattern": "Product was distributed in the following states: Nationwide",
      "state": "OH",
      "product_description": "Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 30 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 68084-887-32; Blister NDC 68084-887-33",
      "report_date": "20160914",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Amerisource Health Services",
      "recall_number": "D-1490-2016",
      "initial_firm_notification": "E-Mail",
      "product_type": "Drugs",
      "event_id": "75076",
      "termination_date": "20171218",
      "more_code_info": "",
      "recall_initiation_date": "20160824",
      "postal_code": "43217-1188",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}