{
  "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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  "results": [
    {
      "country": "United States",
      "city": "Marietta",
      "address_1": "895 Sawyer Rd",
      "reason_for_recall": "Failed Dissolution Specification:12 hour time point at 18 months of product shelf life.",
      "address_2": "",
      "product_quantity": "57857 bottles",
      "code_info": "Lot #: a) 58975, 58976, 58977, 65165 , Exp 01/14; b) 58973, 58974, 65131, Exp: 01/14",
      "center_classification_date": "20130927",
      "distribution_pattern": "Nationwide",
      "state": "GA",
      "product_description": "Venlafaxine (Venlafaxine Hydrochloride) extended release Tablets, 225 mg, packaged in a) 30- count bottle (NDC 0131-3268-32) and b) 90-count bottle (NDC: 0131-3268-46), Rx only, Manufactured by: Kremers Urban Pharmaceuticals Inc. For: Osmotica Pharmaceutical Corp., Wilmington, NC 28405, USA.",
      "report_date": "20131009",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Osmotica Pharmaceutical Corp",
      "recall_number": "D-1067-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "66226",
      "termination_date": "20140509",
      "more_code_info": "",
      "recall_initiation_date": "20130916",
      "postal_code": "30062",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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