{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Arlington",
      "state": "TX",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "73419",
      "recalling_firm": "Apotex Scientific, Inc",
      "address_1": "2100 Rd To Six Flags Dr",
      "address_2": "",
      "postal_code": "76011",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide, Alaska, Hawaii, and Puerto Rico.",
      "recall_number": "D-1436-2016",
      "product_description": "Duloxetine Delayed-Release Capsules, USP, 60 mg, 30-count bottles, Rx only, Manufactured by  Apotex  Inc, Toronto, Ontario M9L 1T9, Manufactured for Apotex Corp. Weston Florida 33326, NDC 60505-2997-3; UPC # 360505299737;",
      "product_quantity": "605,989 (30 ct) bottles",
      "reason_for_recall": "Failed Dissolution Specification: Out of specification dissolution results when testing product stability.",
      "recall_initiation_date": "20160126",
      "center_classification_date": "20160714",
      "termination_date": "20220615",
      "report_date": "20160720",
      "code_info": "Lot #: KW2167,KY9960, KV9789, KV9788; Exp 02/29/2016;   Lot #: KY9961, Exp 04/30/2016;  Lot #: KX6311, KX6312, KY7795, KX6315, Exp 05/31/2016; Lot #: KX6317, Exp 06/30/2016.",
      "more_code_info": ""
    }
  ]
}