{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Las Vegas",
      "address_1": "5835 S Eastern Ave Ste 101",
      "reason_for_recall": "Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.",
      "address_2": "",
      "product_quantity": "15 vials",
      "code_info": "Lot#: 20180212@22, BUD 03/29/2018; 20180226@64, BUD 04/02/2018.",
      "center_classification_date": "20180417",
      "distribution_pattern": "NV only",
      "state": "NV",
      "product_description": "TM #1 (ALP 5.9/PAPAV 17.65/PHEN 0.59) Injectable solution, packaged in 3 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800",
      "report_date": "20180425",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Partell Specialty Pharmacy",
      "recall_number": "D-0645-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "79619",
      "termination_date": "20190115",
      "more_code_info": "",
      "recall_initiation_date": "20180322",
      "postal_code": "89119-3031",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}