{
  "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": "Sunrise",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "65338",
      "recalling_firm": "Actavis South Atlantic LLC",
      "address_1": "13800 Nw 2nd St Ste 190",
      "address_2": "N/A",
      "postal_code": "33325-6243",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-829-2013",
      "product_description": "Ranitidine Syrup (Ranitidine Oral Solution USP) 15 mg/mL, Rx Only.  Manufactured by VistaPharm, Inc., Birmingham, AL 35242.  Distributed by Actavis Mid Atlantic LLC 1877 Kawai Road, Lincolnton, NC  28092 USA",
      "product_quantity": "A total of 133,968 bottles (units)",
      "reason_for_recall": "Failed Impurity/Degradation Specification; \"Related Compound C\"",
      "recall_initiation_date": "20130515",
      "center_classification_date": "20130730",
      "termination_date": "20140515",
      "report_date": "20130807",
      "code_info": "Lot Numbers:  247900, 251000, 256000, 261200, 263600, 266700, 277100, 280300 and 284300.",
      "more_code_info": ""
    }
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}