{
  "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": "Dayton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "80638",
      "recalling_firm": "PharMEDium Services, LLC",
      "address_1": "36 Stults Rd",
      "address_2": "N/A",
      "postal_code": "08810",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was distributed throughout the United States",
      "recall_number": "D-1043-2018",
      "product_description": "10 mcg/mL Fentanyl Citrate (Preservative Free) in 0.9% Sodium Chloride 250 mL in 250 mL Intravia Bag and 10 mcg/mL Fentanyl Citrate (Preservative Free) in 0.9% Sodium Chloride 100 mL in 150 mL Intravia Bag, PharMEDium Services, LLC.",
      "product_quantity": "230 Intravia Bags",
      "reason_for_recall": "CGMP deviations: Product was released while a hood certification discrepancy was being investigated.",
      "recall_initiation_date": "20180724",
      "center_classification_date": "20180803",
      "termination_date": "20181210",
      "report_date": "20180815",
      "code_info": "Lot 181760013D, 181730007D, Exp 08/09/2018, 09/02/2018"
    }
  ]
}