{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Phoenix",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "80000",
      "recalling_firm": "Vitalab Pharmacy, Inc",
      "address_1": "4045 E Bell Rd Ste 163",
      "address_2": "N/A",
      "postal_code": "85032-2240",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The recalled product was distributed to patients throughout the United States.",
      "recall_number": "D-0729-2018",
      "product_description": "Alprostadil 20 mcg/mL, Sterile injectable, Vitalab Pharmacy, Inc",
      "product_quantity": "2 vials",
      "reason_for_recall": "Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns may not be sufficient to support the aseptic production of certain injectable drug products.",
      "recall_initiation_date": "20180424",
      "center_classification_date": "20180509",
      "termination_date": "20200123",
      "report_date": "20180516",
      "code_info": "Lot #: 02122018@77, Exp 05/13/2018"
    }
  ]
}