{
  "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": {
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      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "Horsham",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "66593",
      "recalling_firm": "Amedra Pharmaceuticals LLC",
      "address_1": "2 Walnut Grove Dr",
      "address_2": "Suite 190",
      "postal_code": "19044-2219",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-385-2014",
      "product_description": "Dexedrine¿ (Dextroamphetamine Sulfate) Spansules¿ Sustained Release Capsules 15mg, 90 count bottle, Rx only, Manufactured by Catalent Pharma Solutions Winchester, KY 40391 for Amedra Pharmaceuticals, LLC Middlesex, NJ 08846, NDC 52054-514-09",
      "product_quantity": "10,992 bottles",
      "reason_for_recall": "Failed Dissolution Specifications: Out of Specification (OOS) test results for Hour-4 at the 32 month CRT Stability Level.",
      "recall_initiation_date": "20131007",
      "center_classification_date": "20131223",
      "termination_date": "20141007",
      "report_date": "20140101",
      "code_info": "Lot#  243459; Exp. 01/14",
      "more_code_info": ""
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}